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Medicom 9510

by AMD Medicom Inc

Medicom 9510 is a Class II device made by AMD Medicom Inc, listed in FDA GUDID since 15 Sep 2016 (UDI-DI 10686864040856), 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 Number10686864040856 UDI-DI Date15 Sep 2016ListedStatusListed 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  • Withdrawn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
Medicom
Generic name
Sterilization packaging, single-use
Model / Ref / Catalog
9510
Primary DI / UDI-DI
10686864040856
FDA product code
KCT
GMDN term
Sterilization packaging, single-use
Device class
Class II
Regulation number
880.6850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Sterilization packaging, single-use

Other devices from AMD Medicom Inc

See all devices from AMD Medicom Inc →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
Other properties (12, all answered No)