FDA UDI In Commercial Distribution 🇺🇸 United States

Piffard Dermal Curette

DI: 00192896107922 · Model: 199-202 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Piffard Dermal Curette
Primary DI
00192896107922
Version / Model
199-202
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-21
Public Version
1
Public Version Date
2021-04-29
Public Version Status
New
Public Device Record Key
709d59b8-cd36-4f58-9da1-cc7ae1dc7df5

Device Description

Piffard Dermal Curette Size 2 Wide Handle Oval Tip

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
HTF CURETTE

GMDN Terms

Code Name
62558 General-purpose curette

Identifiers

Type ID
Primary 00192896107922

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Tip 5 Millimeter
Length 6 Inch