FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780076865 · Model: 3712023 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780076865
Version / Model
3712023
Catalog Number
3712023
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
36fbb1e1-e829-42b1-9264-1f2d0c3ac01c

Device Description

Integra® Hajek-Kofler Antrum Punch, 4 mm Bite,90 Degree Down

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
KAW PUNCH, ANTRUM

GMDN Terms

Code Name
36199 ENT soft-tissue cutting forceps

Identifiers

Type ID
Primary 10381780076865

Customer Contacts