FDA UDI In Commercial Distribution 🇺🇸 United States

WINBERG TENDON KNIFE

DI: 00192896057210 · Model: 1271-157 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WINBERG TENDON KNIFE
Primary DI
00192896057210
Version / Model
1271-157
Catalog Number
1271-157
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-17
Public Version
2
Public Version Date
2020-08-20
Public Version Status
Update
Public Device Record Key
14ae32a1-e9fd-4d69-b7fd-53ef24f59d4a

Device Description

WINBERG TENDON KNIFE

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
HTS KNIFE, ORTHOPEDIC

GMDN Terms

Code Name
37837 Orthopaedic osteotome blade, reusable

Identifiers

Type ID
Primary 00192896057210

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7 Inch