FDA UDI In Commercial Distribution 🇺🇸 United States

SEVERIN LACRIMAL CANNULA

DI: 00192896053205 · Model: 1103-500J · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SEVERIN LACRIMAL CANNULA
Primary DI
00192896053205
Version / Model
1103-500J
Catalog Number
1103-500J
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-04
Public Version
1
Public Version Date
2018-11-05
Public Version Status
New
Public Device Record Key
248e301c-2bb6-4257-9ac1-c4008b2bf1bf

Device Description

SEVERIN LACRIMAL CANNULA CURVED TIP

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
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
HMX Cannula, ophthalmic

GMDN Terms

Code Name
46909 Ophthalmic working-channel cannula, reusable

Identifiers

Type ID
Primary 00192896053205

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 30 Gauge