Impression Coping STTIM4011
Ref STTIM4011T
Impression Coping STTIM4011 (STTIM4011T) is a Class I device made by Megagen Implant Co. Ltd, registered in EUDAMED on 25 Aug 2026 (Basic UDI-DI 880972899231PZ) and listed in FDA GUDID since 23 Jun 2023 (UDI-DI 08806388253753), 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 | Number880972899231PZ 08806388253753 | Date25 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number08806388253753 | Date23 Jun 2023 | StatusListed |
Official records
- EUDAMED public site 880972899231PZ
- AccessGUDID record 08806388253753
Across registries
- EUDAMED Basic UDI-DI 880972899231PZ registered 25 Aug 2026 Active
- FDA GUDID UDI-DI 08806388253753 listed 23 Jun 2023 Listed
Timeline
- Listed FDA GUDID 08806388253753
- Registered EUDAMED 880972899231PZ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Impression Coping
- Generic name
- Dental precision attachment simulator/analog, single-use
- Device name
- Impression
- Model / Ref / Catalog
- STTIM4011T, STTIM4011
- Description
- ST Internal Implant System Ø4/ L=11/ Transfer/ Mini
- Primary DI / UDI-DI
- 08806388253753
- Basic UDI-DI
- 880972899231PZ
- FDA product code
- NDP
- EMDN code
- Q010207 Dental impression devices for prosthetic dentistry
- GMDN term
- Dental precision attachment simulator/analog, single-use
- Device class
- Class I
- Regulation number
- 872.3980
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | STTIM4011T | STTIM4011 |
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