FDA UDI In Commercial Distribution 🇺🇸 United States

JEFFERSON RETRACTOR

DI: 00192896026766 · Model: 230-495 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JEFFERSON RETRACTOR
Primary DI
00192896026766
Version / Model
230-495
Catalog Number
230-495
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-10
Public Version
2
Public Version Date
2022-11-01
Public Version Status
Update
Public Device Record Key
1ea97928-343e-47c3-84b5-cfbe75628be6

Device Description

JEFFERSON RETRACTOR BLUNT BLADES CURVED ARMS

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
GAD Retractor

GMDN Terms

Code Name
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Primary 00192896026766

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 3 x 4 Teeth
Device Size Text, specify 16 Millimeter Tip
Length 5 Inch