Microprime 90-00251
by Zest Anchors, LLC EUDAMEDGUDID
Active
Ref 90-00251
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number081659402D0393H | Date29 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00840481135309 | Date10 Mar 2026 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Certificates
No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.
Recalls
No FDA recalls on record, checked 24 Oct 2026.
Specification
- Trade Name
- Microprime
- Generic Name
- Dental material injection cannula, single-use
- Device Name
- Dispensing Tip
- Model / Reference
- 90-00251
- Primary DI / UDI-DI
- 00840481135309
- Basic UDI-DI
- 081659402D0393H
- FDA Product Code
- EID
- EMDN Code
- Q019006 Dental material application tips and brushes, single-use
- GMDN Term
- Dental material injection cannula, single-use
- Device Class
- Class I
- Regulation Number
- 872.4565
- Market of Registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Other devices from Zest Anchors, LLC
Properties
Other properties (20)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No