Weck IPN028498

Trade name

Weck

Generic name

Scalp clip forceps

Model / Ref / Catalog

IPN028498, 658500

Primary DI / UDI-DI

14026704631800

FDA product code

GDO

GMDN term

Scalp clip forceps

Device class

Class I

Regulation number

878.4800

GUDID distribution status

In Commercial Distribution

Sterilisation method

Moist Heat or Steam Sterilization

Category: Scalp clip forceps

Other devices filed under FDA product code GDO (Applier, surgical, clip).

• AESCULAP PL818R by Aesculap AG
• FORCEPS, SUTURE, AUTO by Hartmann Group, Inc.
• InnoClip TRC-H0000 by Taiwan Surgical Corporation
• SURGICAL DRAPE CLIP #201 by C. Intl.
• 360 HEMOCLIP APPLIERS by Edward Weck, Inc.
• LIGACLIP MULTIPLE CLIP APPLIER by Ethicon Inc.
• TOWEL CLIPS by Dhason Brothers, Inc.
• AESCULAP PL817R by Aesculap AG
• SUTURE CLIP APPLIER/REMOVER by Kinetic Medical Products
• BAYONET HEIFETZ CLIP APPLIERS by Edward Weck, Inc.

• Arrow IPNB00820 Open recall

  Class II

  FDA 510(k) K140110 Active Cleared 27 Mar 2015 GUDID on market

• Arrow IPNB00826 Open recall

  Class II

  FDA 510(k) K140110 Active Cleared 27 Mar 2015 GUDID on market

• Arrow IPNB00822 Open recall

  Class II

  FDA 510(k) K140110 Active Cleared 27 Mar 2015 GUDID on market

• Arrow IPNB00827 Open recall

  Class II

  FDA 510(k) K140110 Active Cleared 27 Mar 2015 GUDID on market

See all devices from Teleflex Incorporated →