Microtrol Sterilisation Services Pvt. Ltd.

FDA Device Registration & Listing · Bangalore Karnataka, IN · Registration 3009609358

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009609358
FEI Number
3009609358
Entity Name
Microtrol Sterilisation Services Pvt. Ltd.
City/State/Country
Bangalore Karnataka, IN
Establishment Address
Plot No. 14, Bommasandra - Jigani, Link Road, Industrial Area, KIADB, Bangalore Karnataka 560105, IN
Establishment Type(s)
Sterilize Medical Device for Another Party (Contract Sterilizer)
Owner / Operator
Microtrol Sterilisation Services Pvt. Ltd. (Owner Number: 10048897)
Owner / Operator Contact Address
308-309, ATL Corporate Park, Saki Vihar Road, Mumbai, IN-MH 400072, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Advance Intermittent Catheter Advance Plus Intermittent Catheter Kit Advance Plus Intermittent Catheter Advance Plus Pocket Cocoon Convective Warming Blanket

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NEU Marker, Radiographic, Implantable General, Plastic Surgery Class 2 878.4300 2023-07-13
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2023-06-20
FCM Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit) Gastroenterology, Urology Class 2 876.5130 2020-01-02
KOD Catheter, Urological Gastroenterology, Urology Class 2 876.5130 2020-01-02
KMF Bandage, Liquid General Hospital Class 1 880.5090 2015-08-24
NEU Marker, Radiographic, Implantable General, Plastic Surgery Class 2 878.4300 2023-07-13
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2023-07-13
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2023-07-13
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2023-07-13
DWJ System, Thermal Regulating Cardiovascular Class 2 870.5900 2016-02-02
NEU Marker, Radiographic, Implantable General, Plastic Surgery Class 2 878.4300 2023-07-13
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2023-07-13
FZP Clip, Implantable General, Plastic Surgery Class 2 878.4300 2023-07-13

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Microtrol Sterilisation Services Pvt. Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3007185216 Microtrol Sterilisation Services Pvt. Ltd. Rewari Haryana, IN

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K172344 Medax Srl Unipersonale Medax Biopsy Systems II (MEDONE, MEDCUT, MEDEM, MEDBONE, MEDLOCK) 2017-11-13
K033719 C.R. Bard, Inc. BARD TIGERTAIL URETERAL CATHETER 2004-02-04
K820239 American Endoscopy, Inc. RETRIEVAL FORCEPS 1982-03-26
K041243 Tyco Healthcare DOVER RED RUBBER ROBINSON CATHETER 2004-07-07
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2024 Bard Peripheral Vascular Inc 2
Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Z-0028-2013 Remington Medical Inc. 2
Automatic Cutting Needles, Soft Tissue Biopsy Needle, NAC-1820M, Sterile, Remington Medical, Inc., 5830 Meadowridge Court, Alpharetta, GA 30005. Prostate Biopsy Needles shall be single use only and are to be used by a Urologist in a healthcare setting to obtain needle biopsies of the prostate. The needles are compatible with the Bard Magnum biopsy instrument. The needles have an echogenic tip for accurate placement under ultrasound guidance and centimeter markings along the cannula to facilitate depth placement.
Z-0042-2014 Atossa Genetics, Inc. 2
Brand: The ForeCYTE Breast Health Test, Mammary Aspiration Specimen Cytology Test (MASCT), MASCT System Kits, Clarity System Kits, MASCT Patient Sample Kits & Clarity Patient Sample Kits Instrument, Biopsy. The MASCT System Kit, Patient Sample Kits, or the Nipple Aspirate Fluid Laboratory Kit has the following codes: PRODUCT CODE: AG-MASCT; AG-FC5; DTG-MASCT, DTG-FC5, and NRLBH-5. PART NUMBER: 9002513; 9002513MD; 9002528; 9002528MD; 9002587; 9002614; and 9002717MD. THE MASCT SYSTEM KIT CONSISTS OF: 1. MASCT Breast Pump; 2. Instructions for Use (IFU); 3. Heating Pad; 4. Timer; 5. Saccomono's Fixative; 6. Nu Prep Gel; 7. Welcome and Training Materials Coversheet; 8. MASCT System Order Form; 9. ForeCYTE Training Video DVD; 10. MASCT System Instructions with pictures - pink; THE PATIENT SAMPLE KIT CONSISTS OF: 1. Two (2) flower assemblies (e.g., filter, filter retainer, and filter holder); 2. Instructions for Use (IFU); 3. Two (2) specimen collection devices; 4. Two (2) breast bags for transporting the specimen collection container; 5. Barcode labels; 6. Saccomono's Fixative; 7. Nu Prep Gel; 8. MASCT System package insert; 9. ForeCYTE Test Requisition Form; 10. Patient Information Sheet; 11. Atossa Patient Information; 12. FED EX Clinical PAK; 13. MASCT System Order Form; 14. FED EX Pouch; 15. FED EX Airbill; Product Usage: The MASCT Device is intended for use in the collection of nipple aspirate fluid for cytological testing. The collected fluid can be used in the determination and/or differentiation of normal versus premalignant versus malignant cells.
Z-0044-2018 Bard Peripheral Vascular Inc 2
BARD MAX-CORE Disposable Core Biopsy Instrument, Product Codes - MC1410, 14 g x 10 cm; MC1616, 16 g x 16 cm; MC1816, 18 g x 16 cm; MC1820, 18 g x 20 cm; MC1825, 18 g x 25 cm. The core needle biopsy device is intended for use in obtaining biopsies from soft tissues.
Z-0010-2013 C.R. Bard, Inc., Urological Division 2
8 Fr. Bardex Pediatric All-Silicone Foley Catheter with a 3cc balloon. The product is packaged individually with 12 units per corrugated case. The product is sold sterile for single use and is used to provide continuous urinary drainage from the bladder.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009609358. Last updated year: 2026. Please use registration number 3009609358 when referencing this establishment in official correspondence.
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