FDA UDI In Commercial Distribution 🇺🇸 United States

RUBIN LATERAL OSTEOTOME

DI: 00192896101456 · Model: 475-756 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RUBIN LATERAL OSTEOTOME
Primary DI
00192896101456
Version / Model
475-756
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-11
Public Version
1
Public Version Date
2020-05-19
Public Version Status
New
Public Device Record Key
6dbf1945-41c5-44dc-9151-a444a2983507

Device Description

RUBIN LATERAL OSTEOTOME

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
Yes
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", "Dry Heat Sterilization"]

Product Codes

Code Name
HWM OSTEOTOME

GMDN Terms

Code Name
12846 Plastic surgery osteotome

Identifiers

Type ID
Primary 00192896101456

Customer Contacts