Vygon 555.01
by Vygon
Vygon 555.01 (00055501) is a Class I device made by Vygon, listed in FDA GUDID since 21 Jun 2021 (UDI-DI 03660812007108), registry data as of 9 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03660812007108 | Date21 Jun 2021 | StatusListed |
Official records
- AccessGUDID record 03660812007108
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Vygon
- Generic name
- Tube/mask breathing circuit connector, single-use, sterile
- Model / Ref / Catalog
- 555.01, 00055501
- Primary DI / UDI-DI
- 03660812007108
- FDA product code
- BZA
- GMDN term
- Tube/mask breathing circuit connector, single-use, sterile
- Device class
- Class I
- Regulation number
- 868.5810
- GUDID distribution status
- In Commercial Distribution
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