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Elmed 52206-01

by Elmed Incorporated

Elmed 52206-01 is a Class II device made by Elmed Incorporated, listed in FDA GUDID since 17 Apr 2017 (UDI-DI 00842180107786), 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 Number00842180107786 UDI-DI Date17 Apr 2017ListedStatusListed 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  • Withdrawn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
52206-01
Primary DI / UDI-DI
00842180107786
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

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)