Welch Allyn, Inc. 901060
by Welch Allyn, Inc. 51 variants
Ref 68NCTPModel 901060
Welch Allyn, Inc. 901060 (68NCTP) is a device classified as Class IIb in the EU and Class II in the US made by Welch Allyn, Inc., registered in EUDAMED on 3 Aug 2026 (Basic UDI-DI B-00732094228618) and listed in FDA GUDID since 3 Jun 2025 (UDI-DI 00732094228618), active as of 25 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-00732094228618 00732094228618 | Date3 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00732094228618 | Date3 Jun 2025 | StatusListed |
Official records
- EUDAMED public site B-00732094228618
- AccessGUDID record 00732094228618
Across registries
- EUDAMED Basic UDI-DI B-00732094228618 registered 3 Aug 2026 Active
- FDA GUDID UDI-DI 00732094228618 listed 3 Jun 2025 Listed
Timeline
- Listed FDA GUDID 00732094228618
- Registered EUDAMED B-00732094228618
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Welch Allyn Connex Vital Signs Monitor EUDAMEDWelch Allyn, Inc. GUDID
- Generic name
- General-purpose multi-parameter bedside monitor
- Device name
- Vital Signs Monitor
- Model / Ref / Catalog
- 901060, 68NCTP
- Primary DI / UDI-DI
- 00732094228618
- Basic UDI-DI
- B-00732094228618
- FDA product code
- MWI
- EMDN code
- Z1203020201 Multi–parameter patient bedside monitors
- GMDN term
- General-purpose multi-parameter bedside monitor
- Device class
- Class IIb EUDAMEDClass II GUDID
- Regulation number
- 870.2300
- 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 IIb | Class II |
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