InterLock Trocar Rev A
by Fujifilm New Development U.S.A., Inc. GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00856853006009 | Date17 May 2017 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- Trade Name
- InterLock Trocar
- Generic Name
- Laparoscopic access cannula, single-use
- Model / Ref / Catalog
- Rev A, 1001
- Primary DI / UDI-DI
- 00856853006009
- FDA Product Code
- GCJ
- GMDN Term
- Laparoscopic access cannula, single-use
- Device Class
- Class II
- Regulation Number
- 876.1500
- Commercial Distribution
- Not in Commercial Distribution
Other devices from Fujifilm New Development U.S.A., Inc.
Properties
Other properties (9)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No