FDA UDI In Commercial Distribution 🇺🇸 United States

SPINAL CURETTE

DI: 00192896101784 · Model: 320-865L · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SPINAL CURETTE
Primary DI
00192896101784
Version / Model
320-865L
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-18
Public Version
1
Public Version Date
2020-05-26
Public Version Status
New
Public Device Record Key
b6d97ddb-21b7-402a-850d-122c02d75eb9

Device Description

Spinal Curette Straight Tip Phenolic 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
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
HTF CURETTE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00192896101784

Customer Contacts

Device Sizes

Type Value Unit Text
Length 12 Inch
Device Size Text, specify Size 5