FDA UDI In Commercial Distribution 🇺🇸 United States

DUBOST RETRACTOR BLADE

DI: 00192896086913 · Model: 2500-503 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DUBOST RETRACTOR BLADE
Primary DI
00192896086913
Version / Model
2500-503
Catalog Number
2500-503
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
3
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
3494cf07-7ba5-4d54-9dc0-def44044b9d0

Device Description

DUBOST RETRACTOR BLADE LARGE

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
["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 00192896086913

Customer Contacts

Device Sizes

Type Value Unit Text
Length 4 Inch
Width 2.375 Inch