FDA UDI In Commercial Distribution 🇺🇸 United States

CASPAR CERVICAL BLADE

DI: 00192896037151 · Model: 416-223 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CASPAR CERVICAL BLADE
Primary DI
00192896037151
Version / Model
416-223
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-07
Public Version
4
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
a2fef821-2d61-423b-8a10-cb545182139e

Device Description

CASPAR CERVICAL BLADE

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
FFO Retractor, Self-Retaining

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Previous B0994162230
Primary 00192896037151

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 70 Millimeter
Width 60 Millimeter