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Elmed 52215-01

by Elmed Incorporated

Elmed 52215-01 is a Class II device made by Elmed Incorporated, listed in FDA GUDID since 5 Dec 2018 (UDI-DI 00842180135628), 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 Number00842180135628 UDI-DI Date5 Dec 2018ListedStatusListed 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  • Withdrawn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
Rigid optical laparoscope
Model / Ref / Catalog
52215-01
Primary DI / UDI-DI
00842180135628
FDA product code
HET
GMDN term
Rigid optical laparoscope
Device class
Class II
Regulation number
884.1720
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Rigid optical laparoscope

Similar devices in this category

Other devices filed under Rigid optical laparoscope.

Other devices from Elmed Incorporated

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (9, all answered No)