FDA UDI Not in Commercial Distribution 🇺🇸 United States

Miltex®

DI: 10381780038276 · Model: 62-303 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Miltex®
Primary DI
10381780038276
Version / Model
62-303
Catalog Number
62-303
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-22
Public Version
6
Public Version Date
2021-01-22
Public Version Status
Update
Public Device Record Key
b1b1438b-13a3-421f-bdcb-1e2883b14782
Distribution End Date
2017-03-20

Device Description

TACK PERFRTN RASPATORY

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
No
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
DZL SCREW, FIXATION, INTRAOSSEOUS

GMDN Terms

Code Name
13291 Plastic surgery file/rasp

Identifiers

Type ID
Secondary H834623030
Primary 10381780038276

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K092855 000