FDA UDI In Commercial Distribution 🇺🇸 United States

Corneal Forceps

DI: 00192896102989 · Model: T14-2101 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Corneal Forceps
Primary DI
00192896102989
Version / Model
T14-2101
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-01
Public Version
1
Public Version Date
2020-07-09
Public Version Status
New
Public Device Record Key
75598a39-27f6-4e3a-94a1-5251de0579ca

Device Description

Pierse Corneal Forceps Straight Long Titanium

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
HNR Forceps, ophthalmic

GMDN Terms

Code Name
62674 Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Primary 00192896102989

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Tip 0.1 Millimeter