SeeStar 13312
by Apriomed AB
SeeStar 13312 is a Class I device made by Apriomed AB, listed in FDA GUDID since 4 Dec 2020 (UDI-DI 07350031353136), not in commercial distribution (GUDID) as of 23 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 | Number07350031353136 | Date4 Dec 2020 | StatusListed |
Official records
- AccessGUDID record 07350031353136
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- SeeStar
- Generic name
- Needle guide, single-use
- Model / Ref / Catalog
- 13312
- Primary DI / UDI-DI
- 07350031353136
- FDA product code
- GDF
- GMDN term
- Needle guide, single-use
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- Not in Commercial Distribution
- Size
- Needle Gauge — 12 Gauge
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