FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Jarit®

DI: 10381780193593 · Model: P5020 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Jarit®
Primary DI
10381780193593
Version / Model
P5020
Catalog Number
P5020
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-03
Public Version
5
Public Version Date
2023-04-21
Public Version Status
Update
Public Device Record Key
60499a50-1162-4a83-beae-c6d04652a522

Device Description

Integra® Jarit® Jaeger Lid Plate, 4-3/8", Double-Ended, Blades 21mm and 24mm, 0.8mm Thickness

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
HNI Retractor, ophthalmic

GMDN Terms

Code Name
35314 Periocular/lacrimal retractor, hand-held, reusable

Identifiers

Type ID
Secondary M274P50201
Primary 10381780193593

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 4-3/8", .8mm Thickness
Device Size Text, specify 21mm and 24mm Blades