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SeeStar 13320

by Apriomed AB

SeeStar 13320 is a Class I device made by Apriomed AB, listed in FDA GUDID since 4 Dec 2020 (UDI-DI 07350031353204), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07350031353204 UDI-DI Date4 Dec 2020ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
SeeStar
Generic name
Needle guide, single-use
Model / Ref / Catalog
13320
Primary DI / UDI-DI
07350031353204
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 — 20 Gauge

Related devices

Category: Needle guide, single-use

Other devices from Apriomed AB

See all devices from Apriomed AB →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)