FDA UDI In Commercial Distribution 🇺🇸 United States

AcroPinch™ Device

DI: 10850828007029 · Model: EN-248 · AXOGEN CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AcroPinch™ Device
Primary DI
10850828007029
Version / Model
EN-248
Company Name
AXOGEN CORPORATION
Labeler DUNS
113424464
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-15
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
75d227c8-15e1-493a-a73b-c060a2abff43

Device Description

Hand dynamometer intended for use with the AcroVal™ Neurosensory & Motor Testing System (NSMTS) to measure the pinch force of a patient’s fingers.

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
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LBB Dynamometer, Ac-Powered

GMDN Terms

Code Name
33785 Hand dynamometer/pinchmeter, electronic

Identifiers

Type ID
Primary 10850828007029

Customer Contacts

Phone
888.296.4361

Premarket Submissions

Submission Number Supplement Number
K914056 000