FDA UDI In Commercial Distribution 🇺🇸 United States

CONVERSE SCISSORS

DI: 00192896015265 · Model: 13-9800 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CONVERSE SCISSORS
Primary DI
00192896015265
Version / Model
13-9800
Catalog Number
13-9800
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-13
Public Version
2
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
f75f49c4-2dce-4225-955a-1ed79df98688

Device Description

CONVERSE SCISSORS CLASSIC UP-ANGLE BLADE

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
HNF SCISSORS, OPHTHALMIC

GMDN Terms

Code Name
13487 Enucleation scissors, reusable

Identifiers

Type ID
Primary 00192896015265

Customer Contacts

Device Sizes

Type Value Unit Text
Length 4 Inch