FDA UDI In Commercial Distribution 🇺🇸 United States

CASPAR SCREWDRIVER

DI: 00192896037250 · Model: 416-330 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CASPAR SCREWDRIVER
Primary DI
00192896037250
Version / Model
416-330
Catalog Number
416-330
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
2
Public Version Date
2020-10-01
Public Version Status
Update
Public Device Record Key
fa5ca42b-a296-4de4-8ce1-6021bb017643

Device Description

CASPAR SCREWDRIVER UNIVERSAL

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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
HXX SCREWDRIVER

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Primary 00192896037250

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7.75 Inch