AccessGUDID - DEVICE: V. Mueller (70885403124022)

GUDID

Device Identifier (DI) Information

Brand Name: V. Mueller
Version or Model: CH13029
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: CH13029
Company Name: CAREFUSION 2200, INC

Primary DI Number: 70885403124022
Issuing Agency: GS1
Commercial Distribution End Date: January 07, 2021
Device Count: 2
Labeler D-U-N-S® Number*: 832696038 *Terms of Use

Device Description: V. Mueller GENERAL PURPOSE CLAMP SINGLE, CURVED, PAIR, BLACK FOR VESSELS FROM 0.3 TO 1MM

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

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
62468	Surgical soft-tissue manipulation forceps, scissors-like, reusable	A hand-held, manual, open-surgery instrument designed to grasp, manipulate, dissect, and/or clamp soft-tissues (e.g., organs, blood vessels); it is not intended for grasping/clamping bone or teeth, nor is it dedicated to ophthalmic surgery and is not a dedicated biopsy device. It has a scissors-like hinged design with ring handles and blades (non-cutting) that may be available in a range of sizes or designs. It may be intended for use at a specific anatomy. This is a reusable device intended to be sterilized prior to use.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DXC	CLAMP, VASCULAR

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

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 Record Status

Public Device Record Key: 0357a24e-ba24-44fd-a73e-e7808f34787e
Public Version Date: March 04, 2022
Public Version Number: 5
DI Record Publish Date: September 30, 2016