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Orchid OR2859-DT

by Quest USA Corp.

Orchid OR2859-DT is a Class I device made by Quest USA Corp., listed in FDA GUDID since 3 Feb 2026 (UDI-DI 00198926007460), 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 Number00198926007460 UDI-DI Date3 Feb 2026ListedStatusListed 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  • Withdrawn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
Orchid
Generic name
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial
Model / reference
OR2859-DT
Primary DI / UDI-DI
00198926007460
FDA product code
NAC
GMDN term
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial
Device class
Class I
Regulation number
878.4018
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NAC (Dressing, Wound, Hydrophilic).

Other devices from Quest USA Corp.

See all devices from Quest USA Corp. →

Properties

  • Single use
  • Premarket exempt
Other properties (13, all answered No)