FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Miltex®

DI: 10381780421863 · Model: 20380 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Miltex®
Primary DI
10381780421863
Version / Model
20380
Catalog Number
20-380
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-12
Public Version
9
Public Version Date
2023-05-23
Public Version Status
Update
Public Device Record Key
2e80e667-3fa0-4774-91fa-b036c5a86ebe

Device Description

Integra® Miltex® Wiener Antrum Rasp, No. 2, Medium, Trocar Tip

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
No

Product Codes

Code Name
KAZ RASP, FRONTAL-SINUS

GMDN Terms

Code Name
42379 Frontal sinus file/rasp

Identifiers

Type ID
Secondary H834203800
Primary 10381780421863

Customer Contacts

Device Sizes

Type Value Unit Text
Width 4 Millimeter
Device Size Text, specify 7-3/4"