FDA UDI In Commercial Distribution 🇺🇸 United States

HAND SURGERY OSTEOTOME

DI: 00192896052673 · Model: 1103-293 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HAND SURGERY OSTEOTOME
Primary DI
00192896052673
Version / Model
1103-293
Catalog Number
1103-293
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-04
Public Version
2
Public Version Date
2019-06-10
Public Version Status
Update
Public Device Record Key
040e55e2-b15c-423f-8abd-6b9989fe8d44

Device Description

HAND SURGERY OSTEOTOME STRAIGHT 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
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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
HWM OSTEOTOME

GMDN Terms

Code Name
12844 Orthopaedic osteotome

Identifiers

Type ID
Primary 00192896052673

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 20 Millimeter Blade
Length 5 Inch