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MedDrain 33100

by Armm Inc.

MedDrain 33100 is a Class I device made by Armm Inc., listed in FDA GUDID since 2 Nov 2018 (UDI-DI 10850082007001), 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 Number10850082007001 UDI-DI Date2 Nov 2018ListedStatusListed 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  • Withdrawn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/centesis drainage receptacle
Model / reference
33100
Primary DI / UDI-DI
10850082007001
FDA product code
KGZ
GMDN term
Closed-wound/centesis drainage receptacle
Device class
Class I
Regulation number
878.4200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Closed-wound/centesis drainage receptacle

Similar devices in this category

Other devices filed under Closed-wound/centesis drainage receptacle.

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)