FDA UDI In Commercial Distribution 🇺🇸 United States

Axonpen

DI: 00860000321303 · Model: AH-50-110 · Clearmind Biomedical Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Axonpen
Primary DI
00860000321303
Version / Model
AH-50-110
Company Name
Clearmind Biomedical Inc.
Labeler DUNS
658832644
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-08
Public Version
2
Public Version Date
2022-02-21
Public Version Status
Update
Public Device Record Key
9bf4bc14-4894-4553-8188-8536e2d6016a

Device Description

Axonpen Endoscope

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GWG Endoscope, Neurological

GMDN Terms

Code Name
63706 Surgical irrigation/aspiration cannula, illuminating, single-use

Identifiers

Type ID
Primary 00860000321303
Package 10860000321300

Premarket Submissions

Submission Number Supplement Number
K201308 000