FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780077046 · Model: 3712042 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780077046
Version / Model
3712042
Catalog Number
3712042
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-17
Public Version
5
Public Version Date
2023-04-18
Public Version Status
Update
Public Device Record Key
9a6f50fc-59cf-4d33-a3bf-1771fa1236e6

Device Description

Integra® Circular, Cutting Punch, 4.5 mm, 60 ° Up

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
Yes
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
KAY PUNCH, NASAL

GMDN Terms

Code Name
36199 ENT soft-tissue cutting forceps

Identifiers

Type ID
Primary 10381780077046

Customer Contacts