Mm-Spot 718
Mm-Spot 718 is a Class I device made by Beekley Corporation, listed in FDA GUDID since 31 Jul 2020 (UDI-DI 00815137022128), 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 | Number00815137022128 | Date31 Jul 2020 | StatusListed |
Official records
- AccessGUDID record 00815137022128
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Mm-Spot
- Generic name
- Radiological image marker, noninvasive, single-use
- Model / reference
- 718
- Primary DI / UDI-DI
- 00815137022128
- FDA product code
- JAC
- GMDN term
- Radiological image marker, noninvasive, single-use
- Device class
- Class I
- Regulation number
- 892.1640
- GUDID distribution status
- In Commercial Distribution
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