FDA UDI In Commercial Distribution 🇺🇸 United States

MICRO FRIEDMAN RONGEUR

DI: 00192896027268 · Model: 315-505S · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MICRO FRIEDMAN RONGEUR
Primary DI
00192896027268
Version / Model
315-505S
Catalog Number
315-505S
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-13
Public Version
4
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
96271584-fde5-4568-b729-e0cddefbbbb9

Device Description

MICRO FRIEDMAN RONGEUR STRAIGHT JAW

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
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
HTX RONGEUR

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Primary 00192896027268

Customer Contacts

Device Sizes

Type Value Unit Text
Length 5.5 Inch