FDA UDI In Commercial Distribution 🇺🇸 United States

CASPAR RETRACTOR FRAME

DI: 00192896037014 · Model: 416-202 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CASPAR RETRACTOR FRAME
Primary DI
00192896037014
Version / Model
416-202
Catalog Number
416-202
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-18
Public Version
3
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
9af41474-e926-415b-8a0e-5513a7e8f3fb

Device Description

CASPAR RETRACTOR FRAME ROTATBLE ARMS CERVIC VERTEBRAL COLUMN DOUBLE ARTICULATION

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
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
Primary 00192896037014

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 90 Millimeter Spread