FDA UDI In Commercial Distribution 🇺🇸 United States

GRACEY CURETTE

DI: 00192896050389 · Model: 1102-RESCGR11-14 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GRACEY CURETTE
Primary DI
00192896050389
Version / Model
1102-RESCGR11-14
Catalog Number
1102-RESCGR11-14
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
2019-09-09
Public Version Status
Update
Public Device Record Key
0b9fcc6a-e575-4a73-b3a7-bb9e9ac85a66

Device Description

GRACEY CURETTE #11-14 DOUBLE ENDED 11-MESIAL/14-DISTAL LIGHT 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
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 00192896050389

Customer Contacts