Hdmi Cable Maj-2551
by Olympus Medical Systems Corporation
Ref N6217700
Hdmi Cable Maj-2551 (N6217700) 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 495317000101AW), cleared under FDA 510(k) K243380 on 3 Mar 2025 and listed in FDA GUDID since 17 Mar 2025 (UDI-DI 04953170458255), 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 | Number495317000101AW 04953170458255 | Date23 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04953170458255 | Date17 Mar 2025 | StatusListed |
| United States | FDA 510(k)SESE GUDID | NumberK243380 | Date3 Mar 2025 | StatusActive |
Official records
- EUDAMED public site 495317000101AW
- AccessGUDID record 04953170458255
- FDA 510(k) database K243380
Across registries
- EUDAMED Basic UDI-DI 495317000101AW registered 23 Oct 2026 Active
- FDA 510(k) K243380 decided 3 Mar 2025 Active
- FDA GUDID UDI-DI 04953170458255 listed 17 Mar 2025 Listed
Timeline
- Cleared FDA 510(k) K243380
- Listed FDA GUDID 04953170458255
- Registered EUDAMED 495317000101AW
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Hdmi Cable Maj-2551 EUDAMEDHdmi Cable GUDID
- Generic name
- Electrical-only medical device connection cable, reusable
- Device name
- Cable_Instruments For The Acquisition And Management Of Endoscopic And Minimally Invasive Surgery Images
- Model / Ref / Catalog
- N6217700, MAJ-2551
- Primary DI / UDI-DI
- 04953170458255
- Basic UDI-DI
- 495317000101AW
- 510(k) Number
- FDA product code
- EOB, EOQ, NWB, EQL, NTN, HET
- EMDN code
- Z12020480 Instruments for the acquisition and management of endoscopic and minimally invasive surgery images - hardware accessories
- GMDN term
- Electrical-only medical device connection cable, reusable
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 874.4760, 874.4680, 876.1500, 874.4750, 884.1720
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | N6217700 | MAJ-2551 |
| Device class | Class I | Class II |
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