FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Jarit®

DI: 10381780199106 · Model: 410123 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Jarit®
Primary DI
10381780199106
Version / Model
410123
Catalog Number
410-123
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-23
Public Version
5
Public Version Date
2023-04-19
Public Version Status
Update
Public Device Record Key
c03606f2-3fdc-4254-841b-b52640d4f043

Device Description

Integra® Jarit® Converse Bistoury 6-1/2", Button End, Curved, 5.8mm wide Blade

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
Yes
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
KTG KNIFE, ENT

GMDN Terms

Code Name
38103 Nasal knife

Identifiers

Type ID
Secondary M2744101231
Primary 10381780199106

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 6-1/2"
Device Size Text, specify 5.8mm Wide Blade