Duplotip 0600036
Duplotip 0600036 is an open-surgery adhesive/sealant applicator (FDA Class II; FDA product code FMF, Syringe, Piston) made by Micromedics, Inc., cleared under FDA 510(k) K033589 on 4 Oct 2004 and listed in FDA GUDID since 25 Sep 2016 (UDI-DI 00815634020092), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00815634020092 | Date25 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK033589 | Date4 Oct 2004 | StatusActive |
Official records
- AccessGUDID record 00815634020092
- FDA 510(k) database K033589
Across registries
- FDA 510(k) K033589 decided 4 Oct 2004 Active
- FDA GUDID UDI-DI 00815634020092 listed 25 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K033589
- Listed FDA GUDID 00815634020092
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Duplotip
- Generic name
- Open-surgery adhesive/sealant applicator, dual-channel
- Model / reference
- 0600036
- Primary DI / UDI-DI
- 00815634020092
- 510(k) Number
- FDA product code
- FMF
- GMDN term
- Open-surgery adhesive/sealant applicator, dual-channel
- Device class
- Class II
- Regulation number
- 880.5860
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Open-surgery adhesive/sealant applicator, dual-channel.