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Motion Medical Distributing 1723

by Haslam Medical, Inc.

Motion Medical Distributing 1723 is a Class II device made by Haslam Medical, Inc., listed in FDA GUDID since 4 Jan 2017 (UDI-DI 15060498451229), 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 Number15060498451229 UDI-DI Date4 Jan 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  • Withdrawn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
Motion Medical Distributing
Generic name
Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use
Model / Ref / Catalog
1723
Primary DI / UDI-DI
15060498451229
FDA product code
OKV
GMDN term
Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use
Device class
Class II
Regulation number
884.4520
GUDID distribution status
In Commercial Distribution

Related devices

Category: Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use

Other devices from Haslam Medical, Inc.

See all devices from Haslam Medical, Inc. →

Properties

  • Single use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)