FDA UDI In Commercial Distribution 🇺🇸 United States

SEVERIN LACRIMAL CANNULA

DI: 00192896083141 · Model: 1103-500G · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SEVERIN LACRIMAL CANNULA
Primary DI
00192896083141
Version / Model
1103-500G
Catalog Number
1103-500G
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-21
Public Version
3
Public Version Date
2019-06-12
Public Version Status
Update
Public Device Record Key
09f816e7-78bf-4c60-858c-7d787eeaf5f0

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

Product Codes

Code Name
HMX Cannula, ophthalmic

GMDN Terms

Code Name
46909 Ophthalmic working-channel cannula, reusable

Identifiers

Type ID
Primary 00192896083141

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 26 Gauge