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Marshall Arthroscopy MM110

by Packroom LLC

Marshall Arthroscopy MM110 is a device made by Packroom LLC, listed in FDA GUDID since 19 Oct 2021 (UDI-DI 00817395022261), 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 Number00817395022261 UDI-DI Date19 Oct 2021ListedStatusListed 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  • Withdrawn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
Marshall Arthroscopy
Generic name
General surgical procedure kit, non-medicated, single-use
Model / reference
MM110
Primary DI / UDI-DI
00817395022261
GMDN term
General surgical procedure kit, non-medicated, single-use
GUDID distribution status
In Commercial Distribution

Related devices

Category: General surgical procedure kit, non-medicated, single-use

Other devices from Packroom LLC

See all devices from Packroom LLC →

Properties

  • Supplied sterile
  • Single use
  • Convenience kit
  • Lot / batch number
Other properties (11, all answered No)