FDA UDI In Commercial Distribution 🇺🇸 United States

SCOVILLE NERVE ROOT RETRACTOR

DI: 00192896036031 · Model: 412-643D · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SCOVILLE NERVE ROOT RETRACTOR
Primary DI
00192896036031
Version / Model
412-643D
Catalog Number
412-643D
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-18
Public Version
2
Public Version Date
2018-12-21
Public Version Status
Update
Public Device Record Key
c452c66a-efc8-4607-98a7-01096cf0752e

Device Description

SCOVILLE NERVE ROOT RETRACTOR BAYONET SHAFT

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
GAD RETRACTOR

GMDN Terms

Code Name
46768 Nerve/vessel retractor

Identifiers

Type ID
Primary 00192896036031

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 8 Millimeter Tip