Namic 91300009
Ref 91300009
Namic 91300009 is a device classified as Class IIa in the EU and Class II in the US made by Medline Industries, Inc., registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI B-10193489069013) and listed in FDA GUDID since 26 Jul 2021 (UDI-DI 10193489069013), active as of 7 Nov 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-10193489069013 10193489069013 | Date27 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10193489069013 | Date26 Jul 2021 | StatusListed |
Official records
- EUDAMED public site B-10193489069013
- AccessGUDID record 10193489069013
Across registries
- EUDAMED Basic UDI-DI B-10193489069013 registered 27 Oct 2026 Active
- FDA GUDID UDI-DI 10193489069013 listed 26 Jul 2021 Listed
Timeline
- Listed FDA GUDID 10193489069013
- Registered EUDAMED B-10193489069013
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- SET,IV,274CM,CHAMBER,IV,NO Vent,st EUDAMEDNamic GUDID
- Generic name
- Basic intravenous administration set, noninvasive
- Device name
- Disposable Stopcocks and Manifolds
- Model / Ref / Catalog
- 91300009
- Primary DI / UDI-DI
- 10193489069013
- Basic UDI-DI
- B-10193489069013
- FDA product code
- FPA
- EMDN code
- A030499 Administration kits - other
- GMDN term
- Basic intravenous administration set, noninvasive
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 880.5440
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 108 Inch
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class II |
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