FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780079361 · Model: 3714222 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780079361
Version / Model
3714222
Catalog Number
3714222
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
3
Public Version Date
2023-04-17
Public Version Status
Update
Public Device Record Key
9e67d54b-c36f-4f11-be6f-1a3adc48baa1

Device Description

Integra® Antrum Curette, 5 mm Round Cup

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
KAP CURETTE, NASAL

GMDN Terms

Code Name
47525 Paranasal sinus curette

Identifiers

Type ID
Primary 10381780079361

Customer Contacts