FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Jarit®

DI: 10381780195993 · Model: 355151 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Jarit®
Primary DI
10381780195993
Version / Model
355151
Catalog Number
355-151
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-02
Public Version
10
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
9c498fc4-accf-4bdf-a0f1-8fbd46b1928d

Device Description

Integra® Jarit® Castroviejo Corneo-Scleral Suture Forceps

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
HNR Forceps, ophthalmic

GMDN Terms

Code Name
62674 Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Secondary M2743551511
Primary 10381780195993

Customer Contacts

Device Sizes

Type Value Unit Text
Width 1 Millimeter
Device Size Text, specify 3-7/8"
Device Size Text, specify 1X2 0.9MM TEETH