FDA UDI In Commercial Distribution 🇺🇸 United States

LENS CUTTER FORCEPS

DI: 00192896095878 · Model: 13-5390 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LENS CUTTER FORCEPS
Primary DI
00192896095878
Version / Model
13-5390
Catalog Number
13-5390
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-09
Public Version
1
Public Version Date
2019-05-17
Public Version Status
New
Public Device Record Key
4ddab3e7-4542-4b4c-9cdd-181846fb5dce

Device Description

LENS CUTTER FORCEPS MCKOOL STYLE 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
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
HNF Scissors, Ophthalmic

GMDN Terms

Code Name
13488 Intraocular scissors, conventional-hinge, reusable

Identifiers

Type ID
Primary 00192896095878

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 4.5 Inch
Device Size Text, specify 1 Millimeter Jaw
Device Size Text, specify 8.5 Millimeter Blade
Device Size Text, specify 0.4 Millimeter Tip