FDA UDI In Commercial Distribution 🇺🇸 United States

FOREMANN K-WIRE DISTRACTOR

DI: 00192896037915 · Model: 417-062 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FOREMANN K-WIRE DISTRACTOR
Primary DI
00192896037915
Version / Model
417-062
Catalog Number
417-062
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-13
Public Version
1
Public Version Date
2018-10-15
Public Version Status
New
Public Device Record Key
ecdadf97-7920-4071-80ee-e19238a08edb

Device Description

FOREMANN K-WIRE DISTRACTOR SMALL CLOSED ARMS

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
HWN INSTRUMENT, COMPRESSION

GMDN Terms

Code Name
56637 Orthopaedic surgical distractor, internal

Identifiers

Type ID
Primary 00192896037915

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6 Inch