FDA UDI In Commercial Distribution 🇺🇸 United States

REPLACEMENT BLADE

DI: 00192896024618 · Model: 199-172 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REPLACEMENT BLADE
Primary DI
00192896024618
Version / Model
199-172
Catalog Number
199-172
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-17
Public Version
3
Public Version Date
2023-06-21
Public Version Status
Update
Public Device Record Key
34f8640a-45ba-49c4-8501-b961039fed7f

Device Description

REPLACEMENT BLADE FOR FINGER RING CUTTER CHROME

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
FNS Ring Cutter

GMDN Terms

Code Name
13399 Ring cutter

Identifiers

Type ID
Primary 00192896024618

Customer Contacts