FDA UDI In Commercial Distribution 🇺🇸 United States

Sideport Nucleus Manipulator

DI: 00192896102910 · Model: T12-1470 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sideport Nucleus Manipulator
Primary DI
00192896102910
Version / Model
T12-1470
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-30
Public Version
1
Public Version Date
2020-07-08
Public Version Status
New
Public Device Record Key
ad3d66bc-bc5c-4b29-8a79-fbeace640514

Device Description

Jarret Sideport Nucleus Manipulator 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
HNA Spud, ophthalmic

GMDN Terms

Code Name
46549 Eye spud/needle

Identifiers

Type ID
Primary 00192896102910

Customer Contacts