FDA UDI In Commercial Distribution 🇺🇸 United States

Cloward Cervical Retractor Frame

DI: 00192896106741 · Model: 416-131 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cloward Cervical Retractor Frame
Primary DI
00192896106741
Version / Model
416-131
Catalog Number
416-131
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-10
Public Version
3
Public Version Date
2023-03-15
Public Version Status
Update
Public Device Record Key
f265f21c-7821-46e8-adb8-85925559712a

Device Description

Cloward Cervical Retractor Frame Only

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

Product Codes

Code Name
GAD RETRACTOR

GMDN Terms

Code Name
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Primary 00192896106741

Customer Contacts