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Cosmea normal

by W. Pelz GmbH & Co. KG 3 variants

Cosmea normal is a Class II device made by W. Pelz GmbH & Co. KG, listed in FDA GUDID since 14 Sep 2020 (UDI-DI 04000576042110), 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 Number04000576042110 UDI-DI Date14 Sep 2020ListedStatusListed 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  • Withdrawn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

Trade name
Cosmea
Generic name
Menstrual pad, scented
Model / reference
normal
Primary DI / UDI-DI
04000576042110
FDA product code
HHL
GMDN term
Menstrual pad, scented
Device class
Class II
Regulation number
884.5425
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HHL (Pad, Menstrual, Scented).

Other devices from W. Pelz GmbH & Co. KG

See all devices from W. Pelz GmbH & Co. KG →

Properties

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