Twinfield 2 56920
by OCULUS Optikgeräte Gesellschaft mit beschränkter Haftung
Twinfield 2 56920 is a Class I device made by OCULUS Optikgeräte Gesellschaft mit beschränkter Haftung, listed in FDA GUDID since 1 Dec 2022 (UDI-DI 04049584000040), registry data as of 23 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 | Number04049584000040 | Date1 Dec 2022 | StatusListed |
Official records
- AccessGUDID record 04049584000040
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Twinfield 2
- Generic name
- Perimeter, automatic
- Model / reference
- 56920
- Primary DI / UDI-DI
- 04049584000040
- FDA product code
- HPT, HOO
- GMDN term
- Perimeter, automatic
- Device class
- Class I
- Regulation number
- 886.1605
- GUDID distribution status
- In Commercial Distribution
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