Suction Socket Electrode 13E202=60
by Otto Bock Healthcare Products GmbH
Ref 13E202=60Model 13E202
Suction Socket Electrode 13E202=60 is a device classified as Class I in the EU and Class II in the US made by Otto Bock Healthcare Products GmbH, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 40644110000000013E202JA) and listed in FDA GUDID since 19 Mar 2020 (UDI-DI 04064411004879), active as of 7 Nov 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 | Number40644110000000013E202JA 04064411004879 | Date29 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04064411004879 | Date19 Mar 2020 | StatusListed |
Official records
- EUDAMED public site 40644110000000013E202JA
- AccessGUDID record 04064411004879
Across registries
- EUDAMED Basic UDI-DI 40644110000000013E202JA registered 29 Oct 2026 Active
- FDA GUDID UDI-DI 04064411004879 listed 19 Mar 2020 Listed
Timeline
- Listed FDA GUDID 04064411004879
- Registered EUDAMED 40644110000000013E202JA
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Suction Socket Electrode
- Generic name
- Myoelectric hand prosthesis
- Model / reference
- 13E202=60, 13E202
- Primary DI / UDI-DI
- 04064411004879
- Basic UDI-DI
- 40644110000000013E202JA
- FDA product code
- GXY
- EMDN code
- N010101 Electromyographic electrodes
- GMDN term
- Myoelectric hand prosthesis
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 882.1320
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class I | Class II |
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