FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Miltex®

DI: 10381780418559 · Model: 18-970 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Miltex®
Primary DI
10381780418559
Version / Model
18-970
Catalog Number
18-970
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-21
Public Version
9
Public Version Date
2024-01-11
Public Version Status
Update
Public Device Record Key
46ccdf1c-e436-4cde-be66-1c3a8c7a99db

Device Description

Integra® Miltex® Wills Hospital Utility Forceps, Cross-Serrated

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HNR Forceps, ophthalmic

GMDN Terms

Code Name
62674 Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Secondary H834189700
Primary 10381780418559

Customer Contacts

Device Sizes

Type Value Unit Text
Length 4 Inch
Width 1.25 Millimeter