AccessGUDID - DEVICE: V. Mueller (10885403028076)

GUDID

Device Identifier (DI) Information

Brand Name: V. Mueller
Version or Model: CH5625
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: CH5625
Company Name: STERIS CORPORATION

Primary DI Number: 10885403028076
Issuing Agency: GS1
Commercial Distribution End Date: November 06, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 021599373 *Terms of Use

Device Description: V. Mueller MERZ AORTA PUNCH STRAIGHT PUNCH SIZE 5MM OVERALL LENGTH 8-1/2 inches 21.6CM

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?
35285	Aorta punch, reusable	A manual surgical instrument designed to cut a circular plug of tissue from the wall of the aorta to create an anastomosis site during vascular surgery. It consists of a pointed, cone-shaped, disk-like tip on the end of a plunger that is inserted through a small incision made; its diameter corresponds to the size of the hole. Behind the tip is a thinner section which entraps (holds) the tissue as the sharp circular blade is pressed down the plunger by the surgeon into and through the tissue. It is typically made of high-grade stainless steel and is available in various punch sizes. It can equally be used to punch holes in other vessels if needed. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DWS	INSTRUMENTS, SURGICAL, CARDIOVASCULAR

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes 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: 56df71ed-8431-476b-ae59-9ebfda00c95b
Public Version Date: November 07, 2024
Public Version Number: 5
DI Record Publish Date: August 09, 2018