FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Jarit®

DI: 10381780136323 · Model: 510220 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Jarit®
Primary DI
10381780136323
Version / Model
510220
Catalog Number
510-220
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-14
Public Version
6
Public Version Date
2023-04-25
Public Version Status
Update
Public Device Record Key
639f94bc-e400-4e82-8f11-55f71e9c5852

Device Description

Integra® Jarit® Simpson Obstetrical 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
HDA Forceps, obstetrical

GMDN Terms

Code Name
35082 Obstetrical forceps, reusable

Identifiers

Type ID
Secondary M2745102201
Primary 10381780136323

Customer Contacts