FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Jarit®

DI: 10381780184034 · Model: 240198 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Jarit®
Primary DI
10381780184034
Version / Model
240198
Catalog Number
240-198
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-29
Public Version
6
Public Version Date
2023-07-28
Public Version Status
Update
Public Device Record Key
e0355ef5-85ff-49aa-8833-65e725103ffd

Device Description

Integra® Jarit® Boyes-Goodfellow Hook, Modified Points

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
33542 Bone hook

Identifiers

Type ID
Secondary M2742401981
Primary 10381780184034

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 8-1/2"