FDA UDI Not in Commercial Distribution 🇺🇸 United States

Integra® Miltex®

DI: 10381780480433 · Model: 700001-0001-001 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Integra® Miltex®
Primary DI
10381780480433
Version / Model
700001-0001-001
Catalog Number
700001-0001-001
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2018-07-03
Public Version
3
Public Version Date
2020-11-02
Public Version Status
Update
Public Device Record Key
6fd332b2-4f44-4d72-898d-84bbbac49a2c
Distribution End Date
2020-03-31

Device Description

Precision™ Parallel Sided Post, Size 3, Titanium, Vented - 10 Pack

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
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
ELR POST, ROOT CANAL

GMDN Terms

Code Name
38609 Root canal post, preformed

Identifiers

Type ID
Secondary H83470000100010011
Primary 10381780480433
Unit of Use 00381780480436

Customer Contacts