FDA UDI Not in Commercial Distribution 🇺🇸 United States

CASPAR CERVICAL BLADE

DI: B0994162230 · Model: 416-223 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
CASPAR CERVICAL BLADE
Primary DI
B0994162230
Version / Model
416-223
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
eef92e97-9d02-4eb1-a2e3-be74689c1e72
Distribution End Date
2018-09-22

Device Description

CASPAR CERVICAL 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 B0994162230

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Width 60 Millimeter
Length 70 Millimeter