AchilloCordPLUS 102-1144
by Xiros Ltd
AchilloCordPLUS 102-1144 is a Class II device made by Xiros Ltd, listed in FDA GUDID since 9 Oct 2015 (UDI-DI 05060267130563), not in commercial distribution (GUDID) as of 22 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 | Number05060267130563 | Date9 Oct 2015 | StatusListed |
Official records
- AccessGUDID record 05060267130563
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- AchilloCordPLUS
- Generic name
- Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
- Model / Ref / Catalog
- 102-1144
- Primary DI / UDI-DI
- 05060267130563
- FDA product code
- GAT
- GMDN term
- Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
- Device class
- Class II
- Regulation number
- 878.5000
- GUDID distribution status
- Not in Commercial Distribution
- MRI safety
- MR Conditional
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