FDA UDI In Commercial Distribution 🇺🇸 United States

KASDAN RETRACTOR

DI: 00192896100039 · Model: 10-4281 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KASDAN RETRACTOR
Primary DI
00192896100039
Version / Model
10-4281
Catalog Number
10-4281
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-05
Public Version
1
Public Version Date
2019-11-13
Public Version Status
New
Public Device Record Key
628dd5c9-3a05-4a75-8c93-2a05bace1630

Device Description

KASDAN RETRACTOR DOUBLE ENDED TIPS BLUE ELECTRO COATED

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
Yes
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
HNI Retractor, Ophthalmic

GMDN Terms

Code Name
35349 Eyelid speculum, reusable

Identifiers

Type ID
Primary 00192896100039

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 6.25 Inch
Device Size Text, specify 19 x 19.5 Millimeter Tip
Device Size Text, specify 13 x 6.5 Millimeter Tip