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Curaplex 8600-01470

by Bound Tree Medical, LLC

Curaplex 8600-01470 is a Class II device made by Bound Tree Medical, LLC, listed in FDA GUDID since 30 Nov 2020 (UDI-DI 00812277036770), 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 Number00812277036770 UDI-DI Date30 Nov 2020ListedStatusListed 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  • Withdrawn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
Blood collection set, noninvasive
Model / Ref / Catalog
8600-01470
Primary DI / UDI-DI
00812277036770
FDA product code
JKA
GMDN term
Blood collection set, noninvasive
Device class
Class II
Regulation number
862.1675
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood collection set, noninvasive

Similar devices

Other devices filed under FDA product code JKA (Tubes, vials, systems, serum separators, blood collection).

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)