FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780075004 · Model: 1458232 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Integra®
Primary DI
10381780075004
Version / Model
1458232
Catalog Number
1458232
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
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
a42ce260-b230-46a4-bb58-926634da4b2a

Device Description

Integra® Micro ENT Blade,Straight Blade, Angled Shaft

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KTG KNIFE, ENT

GMDN Terms

Code Name
37445 Manual scalpel blade, single-use

Identifiers

Type ID
Primary 10381780075004
Unit of Use 00381780075007

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is damaged