FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® MicroFrance®

DI: 10381780097068 · Model: CEV9624I · INTEGRA MICROFRANCE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Integra® MicroFrance®
Primary DI
10381780097068
Version / Model
CEV9624I
Catalog Number
CEV9624I
Company Name
INTEGRA MICROFRANCE
Labeler DUNS
276593071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-04
Public Version
5
Public Version Date
2023-04-26
Public Version Status
Update
Public Device Record Key
764400af-ca46-414c-847c-4c6dc91d293f

Device Description

Integra® MicroFrance® Serrated jaws insert for tube 5 mm diameter, 410 mm length

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
No
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
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
33596 Endoscopic electrosurgical handpiece/electrode, monopolar, reusable

Identifiers

Type ID
Primary 10381780097068

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K993655 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a clean, dry area