FDA UDI In Commercial Distribution 🇺🇸 United States

TOMOCAP

DI: 04059237000747 · Model: N/A · Heidelberg Engineering GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
TOMOCAP
Primary DI
04059237000747
Version / Model
N/A
Catalog Number
18829
Company Name
Heidelberg Engineering GmbH
Labeler DUNS
329833875
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2020-10-29
Public Version
2
Public Version Date
2021-07-19
Public Version Status
Update
Public Device Record Key
631fa9f1-75fa-4c36-9bba-b2b6f54f2e1f

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
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MXK Device, Analysis, Anterior Segment

GMDN Terms

Code Name
45729 Eye anterior segment analyser

Identifiers

Type ID
Primary 04059237000747
Unit of Use 04059237000860