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Curaplex 3271-62602

by Bound Tree Medical, LLC

Curaplex 3271-62602 is a basic bed sheet (FDA Class I; FDA product code KME, Bedding, Disposable, Medical) made by Bound Tree Medical, LLC, listed in FDA GUDID since 30 Jul 2024 (UDI-DI 00810094576509), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810094576509 UDI-DI Date30 Jul 2024ListedStatusListed 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  • Withdrawn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
Curaplex
Generic name
Basic bed sheet, single-use
Model / Ref / Catalog
3271-62602
Primary DI / UDI-DI
00810094576509
FDA product code
KME
GMDN term
Basic bed sheet, single-use
Device class
Class I
Regulation number
880.6060
GUDID distribution status
In Commercial Distribution

Related devices

Category: Basic bed sheet, single-use

Similar devices

Other devices filed under FDA product code KME (BEDDING, DISPOSABLE, MEDICAL).

Other devices from Bound Tree Medical, LLC

See all devices from Bound Tree Medical, LLC →

Properties

  • Premarket exempt
Other properties (14, all answered No)