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BlackJack XF2

by Hatchmed Corporation

BlackJack XF2 is a Class I device made by Hatchmed Corporation, listed in FDA GUDID since 1 Sep 2022 (UDI-DI 00850042446157), 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 Number00850042446157 UDI-DI Date1 Sep 2022ListedStatusListed 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  • Withdrawn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
BlackJack
Generic name
Electrical-only medical device connection cable, reusable
Model / reference
XF2
Primary DI / UDI-DI
00850042446157
FDA product code
ISN
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class I
Regulation number
890.3420
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrical-only medical device connection cable, reusable

Other devices from Hatchmed Corporation

See all devices from Hatchmed Corporation →

Properties

  • Premarket exempt
  • Manufacturing date
Other properties (13, all answered No)