FDA UDI In Commercial Distribution 🇺🇸 United States

Tumark Eye

DI: 04250195612168 · Model: 351290 · SOMATEX Medical Technologies GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Tumark Eye
Primary DI
04250195612168
Version / Model
351290
Catalog Number
351290
Company Name
SOMATEX Medical Technologies GmbH
Labeler DUNS
341679629
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-15
Public Version
1
Public Version Date
2025-07-23
Public Version Status
New
Public Device Record Key
96c054c1-31f7-4b19-acab-76f55ab9a674

Device Characteristics

Single Use
Yes
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NEU Marker, Radiographic, Implantable

GMDN Terms

Code Name
40808 Radiological image marker, implantable

Identifiers

Type ID
Package 14250195612165
Primary 04250195612168
Package 24250195612162