Delta 30 UV 00
by Heine Optotechnik GmbH & Co. KG
Ref 237311
Delta 30 UV 00 is a Class I device made by Heine Optotechnik GmbH & Co. KG, registered in EUDAMED on 29 Sep 2026 (Basic UDI-DI 4053755_D_05_WB) and listed in FDA GUDID since 2 Mar 2026 (UDI-DI 04053755202690), active as of 24 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number4053755_D_05_WB 04053755202690 | Date29 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04053755202690 | Date2 Mar 2026 | StatusListed |
Official records
- EUDAMED public site 4053755_D_05_WB
- AccessGUDID record 04053755202690
Across registries
- EUDAMED Basic UDI-DI 4053755_D_05_WB registered 29 Sep 2026 Active
- FDA GUDID UDI-DI 04053755202690 listed 2 Mar 2026 Listed
Timeline
- Listed FDA GUDID 04053755202690
- Registered EUDAMED 4053755_D_05_WB
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Delta 30 UV
- Generic name
- Dermatoscope, optical
- Model / reference
- 237311 EUDAMED00 GUDID
- Primary DI / UDI-DI
- 04053755202690
- Basic UDI-DI
- 4053755_D_05_WB
- Direct marketing DI
- 04053755202690
- FDA product code
- KYT
- EMDN code
- Z12040108 Dermatoscopes
- GMDN term
- Dermatoscope, optical
- Device class
- Class I
- Regulation number
- 880.6350
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 237311 | 00 |
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