Receiver Dish Cable Maj-1875
by Olympus Medical Systems Corporation
Part of a family of 54 devices: see the family page
Ref N3806300
Receiver Dish Cable Maj-1875 is a device classified as Class I in the EU and Class II in the US made by Olympus Medical Systems Corporation, registered in EUDAMED on 23 Oct 2026 (Basic UDI-DI 495317000153BH), cleared under FDA 510(k) K103312 on 12 May 2011 and listed in FDA GUDID since 21 Sep 2016 (UDI-DI 04953170305696), active as of 7 Nov 2026.
Active
CE MDR 510(k)
Valid until
No date given
FDA recalls
None found
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number495317000153BH 04953170305696 | Date23 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04953170305696 | Date21 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE GUDID | NumberK103312 | Date12 May 2011 | StatusActive |
Official records
- EUDAMED public site 495317000153BH
- AccessGUDID record 04953170305696
- FDA 510(k) database K103312
Across registries
- EUDAMED Basic UDI-DI 495317000153BH registered 23 Oct 2026 Active
- FDA 510(k) K103312 decided 12 May 2011 Active
- FDA GUDID UDI-DI 04953170305696 listed 21 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K103312
- Listed FDA GUDID 04953170305696
- Registered EUDAMED 495317000153BH
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Receiver Dish Cable Maj-1875 EUDAMEDReceiver Dish Cable GUDID
- Generic name
- Electrical-only medical device connection cable, reusable
- Device name
- Electrical-Only Medical Device Connection Cable, Reusable
- Model / reference
- N3806300 EUDAMEDMAJ-1875 GUDID
- Primary DI / UDI-DI
- 04953170305696
- Basic UDI-DI
- 495317000153BH
- FDA product code
- FDF
- EMDN code
- Z12029080 Various instruments for endoscopy and mini-invasive surgery - hardware accessories
- GMDN term
- Electrical-only medical device connection cable, reusable
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 876.1500
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | N3806300 | MAJ-1875 |
| Device class | Class I | Class II |
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