Pachymetry probe 14610-0107
Pachymetry probe 14610-0107 is a Class II device made by Nidek Co., Ltd., listed in FDA GUDID since 10 Jul 2023 (UDI-DI 04987669200094), registry data as of 12 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04987669200094 | Date10 Jul 2023 | StatusListed |
Official records
- AccessGUDID record 04987669200094
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pachymetry probe
- Generic name
- Ultrasound pachymeter
- Model / reference
- 14610-0107
- Primary DI / UDI-DI
- 04987669200094
- FDA product code
- ITX, IYO
- GMDN term
- Ultrasound pachymeter
- Device class
- Class II
- Regulation number
- 892.1570, 892.1560
- GUDID distribution status
- In Commercial Distribution
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