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Spectra

by Uzinmedicare Co., Ltd 27 variants

Spectra is a Class II device made by Uzinmedicare Co., Ltd, listed in FDA GUDID since 16 Jul 2024 (UDI-DI 08809108016522), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

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 Number08809108016522 UDI-DI Date16 Jul 2024ListedStatusListed GUDID: 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  • Withdrawn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

Generic name
Breast pump support kit, reusable
Model / reference
Spectra accessory (SG Portable Bagic Accessory Kit)
Primary DI / UDI-DI
08809108016522
FDA product code
HGX
GMDN term
Breast pump support kit, reusable
Device class
Class II
Regulation number
884.5160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Breast pump support kit, reusable

Other devices from Uzinmedicare Co., Ltd

See all devices from Uzinmedicare Co., Ltd →

Properties

  • Over-the-counter
  • Premarket exempt
  • Manufacturing date
Other properties (12, all answered No)