FDA UDI In Commercial Distribution 🇺🇸 United States

MicroFrance®

DI: 10381780103424 · Model: MCEN62T3 · INTEGRA MICROFRANCE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MicroFrance®
Primary DI
10381780103424
Version / Model
MCEN62T3
Catalog Number
MCEN62T3
Company Name
INTEGRA MICROFRANCE
Labeler DUNS
276593071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-10
Public Version
4
Public Version Date
2023-05-11
Public Version Status
Update
Public Device Record Key
9e9ec7a9-1408-47b0-995e-c692faac8669

Device Description

MicroFrance® Jankowski fenestrated cup forceps, 45 °, 6 mm jaws

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
Yes
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
KAE FORCEPS, ENT

GMDN Terms

Code Name
33442 Craniofacial rongeur, reusable

Identifiers

Type ID
Primary 10381780103424

Customer Contacts