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Medline DYNJP2212P

by Medline Industries, Inc.

Medline DYNJP2212P is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 14 Oct 2016 (UDI-DI 10884389188200), 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 Number10884389188200 UDI-DI Date14 Oct 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  • Withdrawn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
Medline
Generic name
Surgical gown, single-use
Model / Ref / Catalog
DYNJP2212P
Primary DI / UDI-DI
10884389188200
FDA product code
FYA
GMDN term
Surgical gown, single-use
Device class
Class II
Regulation number
878.4040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical gown, single-use

Similar devices

Other devices filed under FDA product code FYA (GOWN, SURGICAL).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Convenience kit
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)