Medex BBF26

• FDA 510(k) K841882 decided 5 Jun 1984 Active
• FDA GUDID UDI-DI 10351688512017 listed 11 Oct 2016 Listed

1. 5 Jun 1984 Cleared FDA 510(k) K841882
2. 11 Oct 2016 Listed FDA GUDID 10351688512017

Trade name

Medex

Generic name

Electric infusion pump administration set, single-use

Model / reference

BBF26

Primary DI / UDI-DI

10351688512017

510(k) Number

K841882 ↗

FDA product code

FPA

GMDN term

Electric infusion pump administration set, single-use

Device class

Class II

Regulation number

880.5440

GUDID distribution status

In Commercial Distribution

Category: Electric infusion pump administration set, single-use

Other devices filed under FDA product code FPA (Set, administration, intravascular).

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• OMNIMED I.V. SOLUTION ADMIN. SET by Omni Intl., Inc.
• I.V. Administration Set, I.V. Extension Set by BQ PLUS MEDICAL CO.,LTD
• CADD ADMINISTRATION SET WITH FLOW STOP, MEDICATION CASSETTE RESERVOIR WITH FLOW STOP AND EXTENSION SET by Smiths Medical MD, Inc.
• OPTFlow OPT22614U by EMED Technologies Corporation
• CARESITE LUER ACCESS DEVICE by B. Braun Medical, Inc.
• LUER-LOK MULTIFLO ADAPTER by Deseret Medical, Inc.

• Bivona FT26JN30NGF219N

  Class II

  FDA 510(k) K923878 Active Cleared 29 Dec 1992 GUDID on market

• Bivona HT26JS70NSC222N

  Class II

  FDA 510(k) K923878 Active Cleared 29 Dec 1992 GUDID on market

• Bivona HT26JS80NSC205N

  Class II

  FDA 510(k) K923878 Active Cleared 29 Dec 1992 GUDID on market

• Bivona ST26JN55NSA204N

  Class II

  FDA 510(k) K923878 Active Cleared 29 Dec 1992 GUDID on market

See all devices from ICU Medical, Inc. →