Pharmamed SA.

FDA Device Registration & Listing · Anderlecht Brussels-Capital Region, BE · Registration 3037918935

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
3037918935
FEI Number
3037918935
Entity Name
Pharmamed SA.
City/State/Country
Anderlecht Brussels-Capital Region, BE
Establishment Address
Boulevard Sylvain Dupuis 280/3, Anderlecht Brussels-Capital Region 1070, BE
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Pharmamed SA. (Owner Number: 10093219)
Owner / Operator Contact Address
Boulevard Sylvain Dupuis 280/3, Anderlecht, BE-NOTA 1070, BE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Speculum, vaginal, nonmetal Protector, ostomy Drape, surgical, exempt Tubes, vials, systems, serum separators, blood collection BANDAGE, ELASTIC Stocking, medical support (to prevent pooling of blood in legs) Circuit, breathing (w connector, adaptor, y piece) Dressing, wound, hydrophilic Elastomer, silicone, for scar management Dressing, wound, drug Tape and bandage, adhesive Bandage, liquid CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE) Tube tracheostomy and tube cuff

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HIB Speculum, Vaginal, Nonmetal Obstetrics/Gynecology Class 2 884.4530 2026-05-12
EXE Protector, Ostomy Gastroenterology, Urology Class 1 876.5900 2026-06-18
PUI Drape, Surgical, Exempt General, Plastic Surgery Class 2 878.4370 2025-07-08
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection Clinical Chemistry Class 2 862.1675 2025-07-08
FQM Bandage, Elastic General Hospital Class 1 880.5075 2026-05-12
DWL Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) General Hospital Class 2 880.5780 2026-06-18
CAI Circuit, Breathing (W Connector, Adaptor, Y Piece) Anesthesiology Class 1 868.5240 2025-04-14
NAC Dressing, Wound, Hydrophilic General, Plastic Surgery Class 1 878.4018 2025-08-22
MDA Elastomer, Silicone, For Scar Management General, Plastic Surgery Class 1 878.4025 2026-06-18
FRO Dressing, Wound, Drug Unknown Class U N/A 2026-05-12
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2025-07-08
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days General Hospital Class 2 880.5200 2025-07-08
KMF Bandage, Liquid General Hospital Class 1 880.5090 2026-06-18
BYD Condenser, Heat And Moisture (Artificial Nose) Anesthesiology Class 1 868.5375 2026-05-12
JOH Tube Tracheostomy And Tube Cuff Anesthesiology Class 2 868.5800 2026-06-18

Official Correspondent

Bruno Glorieux

US Agent Details

Celia Parnicky Business: SSPT Inc Email: manager@airshiptrading.com Phone: (954) 2610657

Related Public Records

Same Entity

Pharmamed SA.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K945777 Smiths Industries Medical Systems, Inc. PRO-VENT(TM), PULSATOR(R), AND LINE DRAW(TM) ARTERIAL BLOOD SAMPLING SYRINGES 1994-12-22
K150256 Argentum Medical SILVERLON BURN CONTACT DRESSINGS 2015-04-30
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0030-2014 Perkin Elmer Health Sciences, Inc. 2
Perkin Elmer 226 Sample Collection Device, Serial numbers: 06132903 - 06198900. The PerkinElmer 226 Sample Collection Devices are intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory, in newborn screening. The device includes a tear-apart form for the collection of demographic information.
Z-0033-04 VIASYS Med Systems 1
Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube with Bird adapter, oxygen supply tubing, sideport connector with adjustable bleed valve, and 40 cm H2O Popoff elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83124-2
Z-0034-04 VIASYS Med Systems 1
Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve, ported elbow and infant mask; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83100-24
Z-0035-04 VIASYS Med Systems 1
Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve, 40 cm H2O Popoff elbow and infant mask; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83144-24
Z-0036-04 VIASYS Med Systems 1
Hyperinflation Circuit, consisting of a 2.0 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve and ported elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83120

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3037918935. Last updated year: 2026. Please use registration number 3037918935 when referencing this establishment in official correspondence.
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