Namic 70058308
Ref 70058308
Namic 70058308 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 20 Oct 2026 (Basic UDI-DI B-10193489065770) and listed in FDA GUDID since 26 Jul 2021 (UDI-DI 10193489065770), active as of 24 Oct 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-10193489065770 10193489065770 | Date20 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10193489065770 | Date26 Jul 2021 | StatusListed |
Official records
- EUDAMED public site B-10193489065770
- AccessGUDID record 10193489065770
Across registries
- EUDAMED Basic UDI-DI B-10193489065770 registered 20 Oct 2026 Active
- FDA GUDID UDI-DI 10193489065770 listed 26 Jul 2021 Listed
Timeline
- Listed FDA GUDID 10193489065770
- Registered EUDAMED B-10193489065770
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Manifold 3V Comp. Rh/on Pg EUDAMEDNamic GUDID
- Generic name
- Invasive-pressure external transducer, single-use
- Device name
- DC323 - NAMIC_Disposable Blood Pressure Transducers
- Model / Ref / Catalog
- 70058308
- Primary DI / UDI-DI
- 10193489065770
- Basic UDI-DI
- B-10193489065770
- FDA product code
- DRS
- EMDN code
- Z1203020301 Invasive blood pressure monitoring instruments
- GMDN term
- Invasive-pressure external transducer, single-use
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 870.2850
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class II |
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