AccessGUDID - DEVICE: Integra® Jarit® (10381780181491)

GUDID

Device Identifier (DI) Information

Brand Name: Integra® Jarit®
Version or Model: 180180
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 180-180
Company Name: INTEGRA LIFESCIENCES PRODUCTION CORPORATION

Primary DI Number: 10381780181491
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 081277700 *Terms of Use

Device Description: Integra® Jarit® Laparatomy Ring, 1"

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?
32098	Laparotomy ring	A surgical instrument designed in the shape of a circular band that is set into the abdominal wall to hold open an incision during surgery on the abdominal organs. It functions as a fixed-length access retractor or wound retractor and is used in procedures where entry of the surgeon's hand into the abdominal cavity may facilitate the procedure, and for the extraction of large specimens. This device is used in colorectal, urological, gynaecological, and general surgical procedures. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FHI	RING, LAPAROTOMY

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: bf88e8e1-c2da-49ca-a91e-379851614325
Public Version Date: April 21, 2023
Public Version Number: 5
DI Record Publish Date: October 31, 2017