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MedDrain 222015

by Armm Inc.

MedDrain 222015 is a Class I device made by Armm Inc., listed in FDA GUDID since 2 Jun 2017 (UDI-DI 10850082007704), 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 Number10850082007704 UDI-DI Date2 Jun 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  • Withdrawn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
MedDrain
Generic name
Closed-wound drain, non-bioabsorbable
Model / reference
222015
Primary DI / UDI-DI
10850082007704
FDA product code
KGZ
GMDN term
Closed-wound drain, non-bioabsorbable
Device class
Class I
Regulation number
878.4200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Closed-wound drain, non-bioabsorbable

Similar devices in this category

Other devices filed under Closed-wound drain, non-bioabsorbable.

Other devices from Armm Inc.

See all devices from Armm Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)