Mark III 130600
Mark III 130600 is a Class I device made by Centrix, Inc., listed in FDA GUDID since 29 Dec 2023 (UDI-DI 00817051023694), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00817051023694 | Date29 Dec 2023 | StatusListed |
Official records
- AccessGUDID record 00817051023694
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Mark III
- Generic name
- Dental material cartridge-plunging applicator, single-component
- Model / reference
- 130600
- Primary DI / UDI-DI
- 00817051023694
- FDA product code
- EID
- GMDN term
- Dental material cartridge-plunging applicator, single-component
- Device class
- Class I
- Regulation number
- 872.4565
- GUDID distribution status
- In Commercial Distribution
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