Morrison Medical 1422BK
Morrison Medical 1422BK is a Class I device made by Morrison Medical, Ltd, listed in FDA GUDID since 1 Oct 2019 (UDI-DI 00647921142220), 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 | Number00647921142220 | Date1 Oct 2019 | StatusListed |
Official records
- AccessGUDID record 00647921142220
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Morrison Medical
- Generic name
- Extrication collar, reusable
- Model / Ref / Catalog
- 1422BK
- Primary DI / UDI-DI
- 00647921142220
- FDA product code
- FMR
- GMDN term
- Extrication collar, reusable
- Device class
- Class I
- Regulation number
- 880.6785
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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