AutoPose Access ABS-101024-1
AutoPose Access ABS-101024-1 is a Class II device made by Bimini Technologies LLC, listed in FDA GUDID since 9 Feb 2022 (UDI-DI 00850034511320), registry data 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 | Number00850034511320 | Date9 Feb 2022 | StatusListed |
Official records
- AccessGUDID record 00850034511320
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- AutoPose Access
- Generic name
- Resective skin contouring/liposuction system depth guide
- Model / reference
- ABS-101024-1
- Primary DI / UDI-DI
- 00850034511320
- FDA product code
- MUU
- GMDN term
- Resective skin contouring/liposuction system depth guide
- Device class
- Class II
- Regulation number
- 878.5040
- GUDID distribution status
- In Commercial Distribution
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