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Curaplex 8600-01349

by Bound Tree Medical, LLC

Curaplex 8600-01349 is a Class II device made by Bound Tree Medical, LLC, listed in FDA GUDID since 15 Dec 2018 (UDI-DI 00812277033014), 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 Number00812277033014 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  • Withdrawn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 vascular intervention infusion catheter
Model / Ref / Catalog
8600-01349
Primary DI / UDI-DI
00812277033014
FDA product code
FOZ
GMDN term
Peripheral vascular intervention infusion catheter
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Peripheral vascular intervention infusion catheter

Similar devices in this category

Other devices filed under Peripheral vascular intervention infusion catheter.

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)