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Spectra Handy Plus

by Uzinmedicare Co., Ltd. 3 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08809108019097 UDI-DI Date15 Oct 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Spectra
Generic Name
Breast pump, manual
Model / Ref / Catalog
Spectra Handy Plus, MM010964
Primary DI / UDI-DI
08809108019097
FDA Product Code
HGY
GMDN Term
Breast pump, manual
Device Class
Class I
Regulation Number
884.5150
GUDID distribution status
In Commercial Distribution

Other devices from Uzinmedicare Co., Ltd.

See all devices from Uzinmedicare Co., Ltd. →

Properties

  • Over-the-Counter
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No