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Elmed 32-10-01E

by Elmed Incorporated

Elmed 32-10-01E is a Class I device made by Elmed Incorporated, listed in FDA GUDID since 14 Sep 2023 (UDI-DI 00842180177352), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00842180177352 UDI-DI Date14 Sep 2023ListedStatusListed 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  • Withdrawn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
Elmed
Generic name
Vaginal speculum, reusable
Model / Ref / Catalog
32-10-01E
Primary DI / UDI-DI
00842180177352
FDA product code
HDF
GMDN term
Vaginal speculum, reusable
Device class
Class I
Regulation number
884.4520
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Vaginal speculum, reusable

Other devices from Elmed Incorporated

See all devices from Elmed Incorporated →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)