FDA UDI Not in Commercial Distribution 🇺🇸 United States

LUCAS DENTAL CURETTE

DI: 00192896052765 · Model: 1103-322 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUCAS DENTAL CURETTE
Primary DI
00192896052765
Version / Model
1103-322
Catalog Number
1103-322
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
2
Public Version Date
2019-03-25
Public Version Status
Update
Public Device Record Key
52e7728a-7adf-4839-b739-2c77f4b5cb65
Distribution End Date
2019-03-22

Device Description

LUCAS DENTAL CURETTE

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
EMK CURETTE, SURGICAL, DENTAL

GMDN Terms

Code Name
41660 Periodontal curette

Identifiers

Type ID
Primary 00192896052765

Customer Contacts