FDA UDI In Commercial Distribution 🇺🇸 United States

Lieberman Speculum

DI: 00192896109155 · Model: T10-1753 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Lieberman Speculum
Primary DI
00192896109155
Version / Model
T10-1753
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-04
Public Version
1
Public Version Date
2021-05-12
Public Version Status
New
Public Device Record Key
e207c661-efad-4e7c-b1e1-a6f5e7262912

Device Description

Lieberman Speculum Nasal Approach 11 Millimeters V-Shaped Blades Small 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
HNC Specula, ophthalmic

GMDN Terms

Code Name
35349 Eyelid speculum, reusable

Identifiers

Type ID
Primary 00192896109155

Customer Contacts