FDA UDI In Commercial Distribution 🇺🇸 United States

LIGHTED SMITH NERVE RETRACTOR

DI: 00192896036086 · Model: 412-723 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LIGHTED SMITH NERVE RETRACTOR
Primary DI
00192896036086
Version / Model
412-723
Catalog Number
412-723
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
3
Public Version Date
2023-06-16
Public Version Status
Update
Public Device Record Key
e3212b5d-fb83-48fb-aedd-1ee6f984be3b

Device Description

LIGHTED SMITH NERVE RETRACTOR

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
FDG Retractor, Fiberoptic

GMDN Terms

Code Name
46768 Nerve/vessel retractor

Identifiers

Type ID
Primary 00192896036086

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 7/1 Millimeter Tip
Device Size Text, specify 5 Inch Working Length
Length 10.75 Inch