baixin KD222

Trade name

baixin

Generic name

Basic intravenous administration set, invasive

Model / reference

KD222

Primary DI / UDI-DI

06936018502424

FDA product code

FPA

GMDN term

Basic intravenous administration set, invasive

Device class

Class II

Regulation number

880.5440

GUDID distribution status

In Commercial Distribution

Sterilisation method

Ethylene Oxide

Other devices filed under FDA product code FPA (Set, Administration, Intravascular).

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• OPTFlow OPT12612U by EMED Technologies Corporation
• SOLUTION ADMINI. SETS- ALTER. DRIP CHAMBER/CONNEC. by Travenol Laboratories, S.A.
• Guerbet 50cm Ext/Inj line Straight CT/MR PN-MDX3205M 240001 by CAIR LGL
• HIgH-Flo™ Needle Set RMS12406 by REPRO MED SYSTEMS, INC.
• EXEL SecureTouch Safety Scalp Vein Set 27708 by Exel International
• NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS by Cardio Med Supplies, Inc.
• BD FlowSmart Set MiniMed Pro-Set by Becton, Dickinson and Company
• WING SAFE INFUSION SET 20 GA, SHS2000 SERIES; WING SAFE INFUSION SET 19 GA, SHS1900 SERIES; WING SAFE INFUSION SET 22 GA by Churchill Medical Systems, Inc.

• Baixin 5ML22GLOCK

  Class II

  FDA 510(k) K083686 Active Cleared 2 Jul 2009 GUDID on market

• Baixin KD204

  Class II

  GUDID on market

• Baixin 3ML23GSLIP

  Class II

  FDA 510(k) K083686 Active Cleared 2 Jul 2009 GUDID on market

• Baixin 1MLLS251

  Class II

  FDA 510(k) K083686 Active Cleared 2 Jul 2009 GUDID on market

See all devices from Anhui Kangda Medical Products Co., Ltd. →