FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Jarit®

DI: 10381780129820 · Model: 440350 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Jarit®
Primary DI
10381780129820
Version / Model
440350
Catalog Number
440-350
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-11
Public Version
9
Public Version Date
2023-04-24
Public Version Status
Update
Public Device Record Key
22e10cea-5863-4bf8-a06f-105ef917e5f0

Device Description

Integra® Jarit® Mckenty Punch, 3-3/8", Rotatable, 2mm Bite

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KTF PUNCH, ENT

GMDN Terms

Code Name
36199 ENT soft-tissue cutting forceps

Identifiers

Type ID
Secondary M2744403501
Primary 10381780129820

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 3-3/8"
Device Size Text, specify 2mm Bite