AccessGUDID - DEVICE: n.a. (04048551106815)

GUDID

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Device Identifier (DI) Information

Brand Name: n.a.
Version or Model: 28164ZBA
Catalog Number:
Company Name: Karl Storz GmbH & Co. KG

Primary DI Number: 04048551106815
Issuing Agency: GS1
Device Count: 1

Device Description: Micro Applying Forceps, WL 10 cm

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

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GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name	GMDN Definition
Surgical clip applier, reusable	A hand-held manual surgical instrument designed to apply small atraumatic clips for the ligation of blood vessels, or similar tubular anatomy, mainly to prevent and/or stop bleeding (i.e., haemostasis) during an open-surgery procedure; it may also be used to apply small clamps (e.g., bulldog type) to tissues. The device is typically a metallic, forceps-like instrument with flat, curved ends to hold and deliver the clips; it may have an interchangeable clip holder containing the clips. This is a reusable device after sterilization.

GMDN Preferred Term Name

GMDN Definition

Surgical clip applier, reusable

A hand-held manual surgical instrument designed to apply small atraumatic clips for the ligation of blood vessels, or similar tubular anatomy, mainly to prevent and/or stop bleeding (i.e., haemostasis) during an open-surgery procedure; it may also be used to apply small clamps (e.g., bulldog type) to tissues. The device is typically a metallic, forceps-like instrument with flat, curved ends to hold and deliver the clips; it may have an interchangeable clip holder containing the clips. This is a reusable device after sterilization.

FDA Product Code

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Product Code	Product Code Name
GWG	ENDOSCOPE, NEUROLOGICAL

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Status

Commercial Distribution Status: In Commercial Distribution
DI Record Publish Date: September 23, 2016
Commercial Distribution End Date:

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

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DEVICE: n.a. (04048551106815)