FDA UDI Not in Commercial Distribution 🇺🇸 United States

CASPAR CERVICAL STANDARD BLADE

DI: B0994162030 · Model: 416-203 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CASPAR CERVICAL STANDARD BLADE
Primary DI
B0994162030
Version / Model
416-203
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-26
Public Version
9
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
8ec1e42b-cb0a-491c-9d8b-db9d33976871
Distribution End Date
2018-09-22

Device Description

CASPAR CERVICAL STANDARD BLADE SET OF 2

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

Product Codes

Code Name
FFO Retractor, Self-Retaining

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary B0994162030

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Width 40 Millimeter
Length 30 Millimeter