FDA UDI In Commercial Distribution 🇺🇸 United States

DISTRACTOR

DI: 00192896037601 · Model: 416-610 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DISTRACTOR
Primary DI
00192896037601
Version / Model
416-610
Catalog Number
416-610
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-10
Public Version
1
Public Version Date
2018-10-11
Public Version Status
New
Public Device Record Key
1b63ec5f-6508-4524-b6c5-3033459d4943

Device Description

DISTRACTOR ANGLED TIP DOUBLE ACTION

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

Product Codes

Code Name
HWN INSTRUMENT, COMPRESSION

GMDN Terms

Code Name
56637 Orthopaedic surgical distractor, internal

Identifiers

Type ID
Primary 00192896037601

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 30 Degree Tip
Length 15 Inch
Device Size Text, specify 0.25 Inch Rod