FDA UDI In Commercial Distribution 🇺🇸 United States

Bone Reduction Clamp

DI: 00192896107540 · Model: 1103-0453 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bone Reduction Clamp
Primary DI
00192896107540
Version / Model
1103-0453
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-14
Public Version
1
Public Version Date
2021-04-22
Public Version Status
New
Public Device Record Key
878e6d03-9be5-474f-b9a5-29aab3968ced

Device Description

Bone Reduction Clamp 12 Millimeters K-Wire 1.8 Millimeter ID Guide With Double Long Ratchet

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

Product Codes

Code Name
HXD CLAMP

GMDN Terms

Code Name
34949 Bone approximation clamp

Identifiers

Type ID
Primary 00192896107540

Customer Contacts

Device Sizes

Type Value Unit Text
Length 8 Inch