VYRSA Pro VYPR-103-009
VYRSA Pro VYPR-103-009 is a Class I device made by Vyrsa Technologies, listed in FDA GUDID since 27 Jan 2024 (UDI-DI G418VYPR1030090), 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 | NumberG418VYPR1030090 | Date27 Jan 2024 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- VYRSA Pro
- Generic name
- Orthopaedic inorganic implant inserter/extractor, reusable
- Model / reference
- VYPR-103-009
- Primary DI / UDI-DI
- G418VYPR1030090
- FDA product code
- LXH
- GMDN term
- Orthopaedic inorganic implant inserter/extractor, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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