FDA UDI In Commercial Distribution 🇺🇸 United States

SMITH PETERSEN OSTEOTOME

DI: 00192896094444 · Model: 330-623 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SMITH PETERSEN OSTEOTOME
Primary DI
00192896094444
Version / Model
330-623
Catalog Number
330-623
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-07
Public Version
1
Public Version Date
2019-03-15
Public Version Status
New
Public Device Record Key
482fa063-bb47-44f4-9a00-474c79e67c76

Device Description

SMITH PETERSEN OSTEOTOME CURVED BLADE

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
No
Has Manufacturing Date
No
Has Expiration Date
Yes
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
HWM OSTEOTOME

GMDN Terms

Code Name
12844 Orthopaedic osteotome

Identifiers

Type ID
Primary 00192896094444

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 0.625 Inch Blade
Length 8 Inch