FDA UDI In Commercial Distribution 🇺🇸 United States

CERCLAGE WIRE TWISTER

DI: 00192896047860 · Model: 1100-496 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CERCLAGE WIRE TWISTER
Primary DI
00192896047860
Version / Model
1100-496
Catalog Number
1100-496
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-14
Public Version
2
Public Version Date
2019-05-16
Public Version Status
Update
Public Device Record Key
f1f04362-8621-4aa6-b064-6b2f76a0e0c5

Device Description

CERCLAGE WIRE TWISTER STAINLESS STEEL

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
HXS TWISTER, WIRE

GMDN Terms

Code Name
32881 Wire twister

Identifiers

Type ID
Primary 00192896047860

Customer Contacts

Device Sizes

Type Value Unit Text
Length 5 Inch