FDA UDI In Commercial Distribution 🇺🇸 United States

CASPAR CERVICAL VERTEBRAL COLUMN RETRACTOR FRAME

DI: 00192896036994 · Model: 416-200 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CASPAR CERVICAL VERTEBRAL COLUMN RETRACTOR FRAME
Primary DI
00192896036994
Version / Model
416-200
Catalog Number
416-200
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-06
Public Version
4
Public Version Date
2023-03-03
Public Version Status
Update
Public Device Record Key
a9242cd2-12f0-47b4-af2a-2a54d2ccea4e

Device Description

CASPAR CERVICAL VERTEBRAL COLUMN RETRACTOR FRAME

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
GAD Retractor

GMDN Terms

Code Name
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Previous B0994162000
Primary 00192896036994

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 120 Millimeter