FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Miltex®

DI: 10381780427759 · Model: 29-102 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Miltex®
Primary DI
10381780427759
Version / Model
29-102
Catalog Number
29-102
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-10
Public Version
6
Public Version Date
2023-04-28
Public Version Status
Update
Public Device Record Key
a143de97-a5ce-45ca-a40a-8d5255b51dc2

Device Description

Integra® Miltex® Mathieu Urethral and IUD Removal Forceps 11-3/4" Shaft, Serrated Jaws 3.5mm x 19mm

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
HHF REMOVER, INTRAUTERINE DEVICE, CONTRACEPTIVE, HOOK-TYPE

GMDN Terms

Code Name
12032 Intrauterine device removal hook, reusable

Identifiers

Type ID
Secondary H834291020
Primary 10381780427759

Customer Contacts