Identity
- Trade Name
- Covidien FDA UDI
- Generic Name
- Medication transfer needle, non-filtering/non-vented FDA UDI
- Device Name
- Grifols 3038172 TRNSF NDL 20X1.625B FDA UDI
- Model / Reference
- 8629091 FDA UDI
- Description
- Grifols 3038172 TRNSF NDL 20X1.625B FDA UDI
Identifiers
- Catalog Number
- 8629091 FDA UDI
- Primary DI / UDI-DI
- 50885380167162 FDA UDI
- FDA Product Code
- GAA FDA UDI
- GMDN Term
- Medication transfer needle, non-filtering/non-vented FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Medication transfer needle, non-filtering/non-vented
Covidien by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Medication transfer needle, non-filtering/non-vented.
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- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- RELI® — MYCO MEDICAL SUPPLIES INC. · Class I
- BD Blunt Fill NRFit — BECTON DICKINSON AND COMPANY · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Cardinalhealth
Sources (1)
- FDA UDI 12101e63-38ba-4848-bbf5-3734f24f0a79 34 fields · synced May 30, 2026