FDA UDI In Commercial Distribution 🇺🇸 United States

Finsen Retractor

DI: 00192896108301 · Model: 220-140 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Finsen Retractor
Primary DI
00192896108301
Version / Model
220-140
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-22
Public Version
1
Public Version Date
2021-04-30
Public Version Status
New
Public Device Record Key
7fa9e4a2-0347-463b-a1f9-c5dae2369cbc

Device Description

Finsen Retractor With Adjustment Screw 3 X 4 Sharp prongs

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

Product Codes

Code Name
GAD RETRACTOR

GMDN Terms

Code Name
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Primary 00192896108301

Customer Contacts

Device Sizes

Type Value Unit Text
Length 2.75 Inch