Portex 4909CS-20

• FDA 510(k) K110053 decided 14 Sep 2012 Active
• FDA GUDID UDI-DI 20351688068429 listed 13 Dec 2016 Listed

1. 14 Sep 2012 Cleared FDA 510(k) K110053
2. 13 Dec 2016 Listed FDA GUDID 20351688068429

Trade name

Portex

Generic name

Epidural anaesthesia set, non-medicated

Model / reference

4909CS-20

Primary DI / UDI-DI

20351688068429

510(k) Number

K110053 ↗

FDA product code

CAZ

GMDN term

Epidural anaesthesia set, non-medicated

Device class

Class II

Regulation number

868.5140

GUDID distribution status

In Commercial Distribution

Category: Epidural anaesthesia set, non-medicated

Other devices filed under FDA product code CAZ (Anesthesia conduction kit).

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• TRAY, AUXILLARY BLOCK by Pharmaseal Div., Baxter Healthcare Corp.
• COSPAN CONTINUOUS SPINAL ANESTHESIA TRAY by Kendall Healthcare Products Co. Div.Of Tyco Health
• CLA KIT (CONTINUOUS LOCAL ANESTHESIA), MODEL 551-17, 551-10, 551-07 by Hdc Corp.
• EPIDURAL ANESTHESIA TRAY by PREFERRED MEDICAL PRODUCTS, LLC
• ANAGO SPINAL ANESTHESIA TRAY by Anago, Inc.
• STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000 by Arrow Intl., 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. →