FDA UDI In Commercial Distribution 🇺🇸 United States

RETI-port/scan 21 basic

DI: 04260157780200 · Model: 20 · Roland Consult Stasche & Finger GmbH
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RETI-port/scan 21 basic
Primary DI
04260157780200
Version / Model
20
Company Name
Roland Consult Stasche & Finger GmbH
Labeler DUNS
314602160
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-26
Public Version
1
Public Version Date
2023-03-06
Public Version Status
New
Public Device Record Key
0f9b4af0-5271-4718-b1b8-a01854c7ad96

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
No
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
GWE Stimulator, Photic, Evoked Response

GMDN Terms

Code Name
11482 Electroretinograph
11480 Electrooculograph

Identifiers

Type ID
Primary 04260157780200

Premarket Submissions

Submission Number Supplement Number
K023525 000