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Curaplex 540-1330EA-A

by Bound Tree Medical, LLC

Curaplex 540-1330EA-A is a peripheral intravenous catheterization support kit (FDA Class II; FDA product code LRS, I.V. start kit) made by Bound Tree Medical, LLC, listed in FDA GUDID since 15 Dec 2018 (UDI-DI 00815277028721), 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 Number00815277028721 UDI-DI Date15 Dec 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  • Withdrawn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
Curaplex
Generic name
Peripheral intravenous catheterization support kit
Model / Ref / Catalog
540-1330EA-A
Primary DI / UDI-DI
00815277028721
FDA product code
LRS
GMDN term
Peripheral intravenous catheterization support kit
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LRS (I.V. start kit).

Other devices from Bound Tree Medical, LLC

See all devices from Bound Tree Medical, LLC →

Properties

  • Single use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)