FDA UDI In Commercial Distribution 🇺🇸 United States

CURETTE

DI: 00192896092372 · Model: 320-881A · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CURETTE
Primary DI
00192896092372
Version / Model
320-881A
Catalog Number
320-881A
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-03
Public Version
2
Public Version Date
2019-05-07
Public Version Status
Update
Public Device Record Key
eff3dc3d-96d0-41a2-b1d1-3453d40c9332

Device Description

CURETTE STRAIGHT TIP CONE RING SIZE 1 PHONELIC HANDLE

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
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00192896092372

Customer Contacts

Device Sizes

Type Value Unit Text
Length 15 Inch