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Covidien

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Covidien FDA UDI
Generic Name
Medication transfer needle, filtering FDA UDI
Device Name
Grifols 3037908 FLTR NDL 16X.75I FDA UDI
Model / Reference
8629121 FDA UDI
Description
Grifols 3037908 FLTR NDL 16X.75I FDA UDI

Identifiers

Catalog Number
8629121 FDA UDI
Primary DI / UDI-DI
50885380167155 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
Medication transfer needle, filtering FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 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

No

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, filtering

Covidien by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medication transfer needle, filtering.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 21c462e7-6d5b-4555-b8ee-b8bb8242f99a 34 fields · synced May 30, 2026