FDA UDI In Commercial Distribution 🇺🇸 United States

DELTA 30 PRO

DI: 04053755201617 · Model: 083 · Heine Optotechnik GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
DELTA 30 PRO
Primary DI
04053755201617
Version / Model
083
Catalog Number
K-235.28.305
Company Name
Heine Optotechnik GmbH & Co. KG
Labeler DUNS
315274563
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-06
Public Version
1
Public Version Date
2024-02-14
Public Version Status
New
Public Device Record Key
589d5e7c-2f12-4555-a4b6-dac33dab2238

Device Description

With Contact Plate

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KYT Light, Examination, Medical, Battery Powered

GMDN Terms

Code Name
18021 Dermatoscope, optical

Identifiers

Type ID
Direct Marking 04053755201549
Primary 04053755201617

Customer Contacts