LAMED PRIVATE LIMITED

FDA Device Registration & Listing · FARIDABAD Haryana, IN · Registration 3042970965

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
3042970965
FEI Number
3042970965
Entity Name
LAMED PRIVATE LIMITED
City/State/Country
FARIDABAD Haryana, IN
Establishment Address
PLOT NO. 136A, SECTOR 24, FARIDABAD Haryana 121005, IN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LAMED PRIVATE LIMITED (Owner Number: 10094725)
Owner / Operator Contact Address
PLOT NO. 136A, SECTOR 24, FARIDABAD, IN-HR 121005, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Closed-ended wearable urine collection bag (U-BAG & U-Meter) Anesthesia Face Mask (La-med Anesthesia Face Mask) Oropharyngeal Airway (La-med- Guedel Airways) Umbilical Cord Clamp (Umbilical Occlusion Device)-Lamed Rebreathing oxygen face mask (O2 mask)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FAQ Bag, Urine Collection, Leg, For External Use, Sterile Gastroenterology, Urology Class 1 876.5250 2025-12-18
BSJ Mask, Gas, Anesthetic Anesthesiology Class 1 868.5550 2025-12-18
CAE Airway, Oropharyngeal, Anesthesiology Anesthesiology Class 1 868.5110 2025-12-18
HFW Clamp, Umbilical Obstetrics/Gynecology Class 2 884.4530 2025-12-18
BYG Mask, Oxygen Anesthesiology Class 1 868.5580 2025-12-18

Official Correspondent

No official correspondent registered.

US Agent Details

Manoj Zacharias Business: LIBERTY MANAGEMENT GROUP LTD Email: office@libertymanagement.us Phone: (630) 2702921

Related Public Records

Same Entity

LAMED PRIVATE LIMITED
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2014 King Systems Corp. 1
King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.

Similar Registrations

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3013557562 CBR ENTERPRISE LIMITED Hong Kong, HK
9710020 ZHEJIANG ANJI HUABU INDUSTRIAL CO., LTD. HUZHOU Zhejiang, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042970965. Last updated year: 2026. Please use registration number 3042970965 when referencing this establishment in official correspondence.
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