FDA UDI In Commercial Distribution 🇺🇸 United States

Kelly-Vernick Retractor Blade

DI: 00192896109056 · Model: 516-951V · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kelly-Vernick Retractor Blade
Primary DI
00192896109056
Version / Model
516-951V
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-30
Public Version
1
Public Version Date
2021-05-10
Public Version Status
New
Public Device Record Key
ec425d5a-d53c-42f8-a1ef-bad902e1cb97

Device Description

Kelly-Vernick Retractor Blade 2.0 Inches X 7.0 Inches Long Lip

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
FFO RETRACTOR, SELF-RETAINING

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 00192896109056

Customer Contacts