FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Miltex®

DI: 10381780496861 · Model: V96-410 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Miltex®
Primary DI
10381780496861
Version / Model
V96-410
Catalog Number
V96-410
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-24
Public Version
5
Public Version Date
2023-05-02
Public Version Status
Update
Public Device Record Key
27d98658-d64f-4c64-bc38-b2f49341d867

Device Description

Integra® Miltex® Splinter Removal Kit, Includes REF# V96-312 and V96-400

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
GEN FORCEPS, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
62466 Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Secondary H834V964100
Primary 10381780496861

Customer Contacts