FDA UDI In Commercial Distribution 🇺🇸 United States

Ring Cannula

DI: 00192896107854 · Model: 16-3990 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ring Cannula
Primary DI
00192896107854
Version / Model
16-3990
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-20
Public Version
1
Public Version Date
2021-04-28
Public Version Status
New
Public Device Record Key
d4434b9e-60d8-4111-93e0-3bd4a770b465

Device Description

Ring Cannula 2 Side Ports 1/3 Turn Separation 1 Millimeter Down 24 Gauge

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
HMX Cannula, ophthalmic

GMDN Terms

Code Name
46909 Ophthalmic working-channel cannula, reusable

Identifiers

Type ID
Primary 00192896107854

Customer Contacts