ILO Swift 1HD USB
Ref 853-0201Model 1Chip (MOS) HD camera system
ILO Swift 1HD USB (853-0201) is a Class I device made by ILO electronic GmbH, registered in EUDAMED on 20 May 2026 (Basic UDI-DI 42503697853P3) and listed in FDA GUDID since 22 Jun 2023 (UDI-DI 04250369706099), active as of 23 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 | Number42503697853P3 04250369706099 | Date20 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04250369706099 | Date22 Jun 2023 | StatusListed |
Official records
- EUDAMED public site 42503697853P3
- AccessGUDID record 04250369706099
Across registries
- EUDAMED Basic UDI-DI 42503697853P3 registered 20 May 2026 Active
- FDA GUDID UDI-DI 04250369706099 listed 22 Jun 2023 Listed
Timeline
- Listed FDA GUDID 04250369706099
- Registered EUDAMED 42503697853P3
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Swift 1HD USB EUDAMEDIlo GUDID
- Generic name
- Endoscope video camera
- Device name
- Endoscopic camera
- Model / Ref / Catalog
- 1Chip (MOS) HD camera system, 853-0201, Swift 1HD USB
- Primary DI / UDI-DI
- 04250369706099
- Basic UDI-DI
- 42503697853P3
- Direct marketing DI
- 04250369706099
- FDA product code
- KQM
- EMDN code
- Z12020405 Surgical cameras
- GMDN term
- Endoscope video camera
- Device class
- Class I
- Regulation number
- 878.4160
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 1Chip (MOS) HD camera system 853-0201 | Swift 1HD USB |
| Sterilise before use | Yes | No |