Velclose S660-LF
Velclose S660-LF is a Class I device made by Tetra Medical Supply Corp., listed in FDA GUDID since 8 Aug 2022 (UDI-DI 00614138124042), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00614138124042 | Date8 Aug 2022 | StatusListed |
Official records
- AccessGUDID record 00614138124042
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Velclose
- Generic name
- Pressure bandage, non-latex, single-use
- Model / Ref / Catalog
- S660-LF
- Primary DI / UDI-DI
- 00614138124042
- FDA product code
- FQM
- GMDN term
- Pressure bandage, non-latex, single-use
- Device class
- Class I
- Regulation number
- 880.5075
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
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