40-8018-044
Ref 40-8018-044
40-8018-044 is a Class I device made by VBM Medizintechnik GmbH, registered in EUDAMED on 12 Mar 2026 (Basic UDI-DI 42501056-2.1.4-VD) and listed in FDA GUDID since 31 Aug 2020 (UDI-DI 04250105601688), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number42501056-2.1.4-VD 04250105601688 | Date12 Mar 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04250105601688 | Date31 Aug 2020 | StatusListed |
Official records
- EUDAMED public site 42501056-2.1.4-VD
- AccessGUDID record 04250105601688
Across registries
- EUDAMED Basic UDI-DI 42501056-2.1.4-VD registered 12 Mar 2026 Active
- FDA GUDID UDI-DI 04250105601688 listed 31 Aug 2020 Listed
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Timeline
- Listed FDA GUDID 04250105601688
- Registered EUDAMED 42501056-2.1.4-VD
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Endotape Length: 54 cm
- Generic name
- Endotracheal tube holder
- Device name
- Tube Fixations - Endotape
- Model / reference
- 40-8018-044
- Primary DI / UDI-DI
- 04250105601688
- Basic UDI-DI
- 42501056-2.1.4-VD
- FDA product code
- CBH
- EMDN code
- R01058099 Tracheostomy and laryngectomy cannulas - various accessories
- GMDN term
- Endotracheal tube holder
- Device class
- Class I
- Regulation number
- 868.5770
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 54 Centimeter
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