FDA UDI In Commercial Distribution 🇺🇸 United States

LESTER LENS PUSHER

DI: 00192896013391 · Model: 12-2980 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LESTER LENS PUSHER
Primary DI
00192896013391
Version / Model
12-2980
Catalog Number
12-2980
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-03
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
c642ec4c-aa1e-43ea-b59f-cb7accd74b6f

Device Description

LESTER LENS PUSHER STRAIGHT TIP STAINLESS STEEL

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
HNQ Hook, ophthalmic

GMDN Terms

Code Name
32754 Ocular hook/spatula/manipulator, reusable

Identifiers

Type ID
Primary 00192896013391

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 0.25 Millimeter