Catalyst Non-Expandable Bed ASM100113
Catalyst Non-Expandable Bed ASM100113 is a Class II device made by Kreg Medical, Inc., listed in FDA GUDID since 21 Sep 2018 (UDI-DI 00850520008143), 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 | Number00850520008143 | Date21 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 00850520008143
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Catalyst Non-Expandable Bed
- Generic name
- Bariatric bed
- Model / reference
- ASM100113
- Primary DI / UDI-DI
- 00850520008143
- FDA product code
- FNL
- GMDN term
- Bariatric bed
- Device class
- Class II
- Regulation number
- 880.5100
- GUDID distribution status
- In Commercial Distribution
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