FDA UDI In Commercial Distribution 🇺🇸 United States

SPINAL DISTRACTOR

DI: 00192896095403 · Model: 416-603 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SPINAL DISTRACTOR
Primary DI
00192896095403
Version / Model
416-603
Catalog Number
416-603
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-07
Public Version
1
Public Version Date
2019-03-15
Public Version Status
New
Public Device Record Key
9ed89565-d7f0-450e-b106-a62faf37af4b

Device Description

SPINAL DISTRACTOR ANGLED

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
No
Has Manufacturing Date
No
Has Expiration Date
Yes
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 00192896095403

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 45 Degree Tip
Length 9.5 Inch