Band Pusher
by American Orthodontics 4 variants
Ref 010-751
Band Pusher (010-751) is an orthodontic metal band pusher (EU MDR Class I; FDA Class I; FDA product code DZN, Instruments, Dental Hand) made by American Orthodontics, registered in EUDAMED on 30 Jul 2025 (Basic UDI-DI 01907460000181DZ) and listed in FDA GUDID since 9 Sep 2020 (UDI-DI 00190746162589), active as of 22 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 | Number01907460000181DZ 00190746162589 | Date30 Jul 2025 | StatusActive |
| United States | GUDID listing GUDID | Number00190746162589 | Date9 Sep 2020 | StatusListed |
Official records
- EUDAMED public site 01907460000181DZ
- AccessGUDID record 00190746162589
Across registries
- EUDAMED Basic UDI-DI 01907460000181DZ registered 30 Jul 2025 Active
- FDA GUDID UDI-DI 00190746162589 listed 9 Sep 2020 Listed
Timeline
- Listed FDA GUDID 00190746162589
- Registered EUDAMED 01907460000181DZ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Band Pusher EUDAMEDGeneral Instruments GUDID
- Generic name
- Orthodontic metal band pusher
- Model / Ref / Catalog
- 010-751
- Description
- INSTRUMENT BAND SEATER/CEMENT SCALER DOUBLE ENDED
- Primary DI / UDI-DI
- 00190746162589
- Basic UDI-DI
- 01907460000181DZ
- FDA product code
- DZN
- EMDN code
- Q010499 Orthodontic devices - other
- GMDN term
- Orthodontic metal band pusher
- Device class
- Class I
- Regulation number
- 872.4565
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Manufacturer details
- EUDAMED SRN
- US-MF-000007702
- Authorised representative
- Medical Technology Promedt Consulting GmbH DE-AR-000000085
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