FDA UDI In Commercial Distribution 🇺🇸 United States

Caspar Medial Blade

DI: 00192896103894 · Model: 416-542 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Caspar Medial Blade
Primary DI
00192896103894
Version / Model
416-542
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-14
Public Version
2
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
935dfe31-1094-42f3-a82f-45e3efe88f63

Device Description

Caspar Medial Blade Quick Release Titanium

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
GAD RETRACTOR

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 00192896103894

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Blade 50 Millimeter x 20 Millimeter