STERiJECT TM PRE-25013I
by Tsk Laboratory, Japan United States GUDID
Product code FMI
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04580708068534 | Date15 Jan 2026 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
-
- Terminated Z-0694-2012
Merz Aesthetics is initiating a medical device recall on TSK Closed Tip Cannula (27GA x 25mm) due to a labeling error on the secondary (outer) packaging. The outer package label states that the carton contains Cannulas that are 27GA x 25 mm in size instead of 27G x 38 mm. Length of the cannula is a matter of user preference and is unlikely to impact patient safety.
Specification
- Trade Name
- STERiJECT TM
- Generic Name
- Hypodermic needle, single-use
- Model / Reference
- PRE-25013I
- Primary DI / UDI-DI
- 04580708068534
- 510(k) Number
- FDA Product Code
- FMI
- GMDN Term
- Hypodermic needle, single-use
- Device Class
- Class II
- Regulation Number
- 880.5570
- Commercial Distribution
- In Commercial Distribution
- Size
- Outer Diameter — 0.5 MillimeterLength — 13 Millimeter
Other devices from Tsk Laboratory, Japan
Properties & raw data
Show properties, registry sources and raw records
Other properties (8)
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
Sources (1)
- FDA UDI 9cb096ea-0771-4606-9b41-4932539491ee