FDA UDI Not in Commercial Distribution 🇺🇸 United States

Alpine BioMed

DI: 00613994242297 · Model: 9031A006501 · Alpine Biomed ApS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Alpine BioMed
Primary DI
00613994242297
Version / Model
9031A006501
Company Name
Alpine Biomed ApS
Labeler DUNS
311231554
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-23
Public Version
5
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
fc03dc7d-d5be-4fd3-8cca-0d2c149664a9
Distribution End Date
2020-04-28

Device Description

KEYPOINT WS UKXP-OS

Device Characteristics

Single Use
No
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
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
GWF Stimulator, Electrical, Evoked Response

GMDN Terms

Code Name
11474 Electromyograph

Identifiers

Type ID
Primary 00613994242297

Premarket Submissions

Submission Number Supplement Number
K944547 000