FDA UDI Not in Commercial Distribution 🇺🇸 United States

ER

DI: 10850390007311 · Model: ER · BTE TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ER
Primary DI
10850390007311
Version / Model
ER
Company Name
BTE TECHNOLOGIES, INC.
Labeler DUNS
021461470
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-25
Public Version
4
Public Version Date
2020-03-04
Public Version Status
Update
Public Device Record Key
2735e69b-e002-4bea-86c2-88790f0308f2
Distribution End Date
2019-12-19

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IKK System, Isokinetic Testing And Evaluation

GMDN Terms

Code Name
63457 Biomechanical function analysis system, force-testing, stationary

Identifiers

Type ID
Primary 10850390007311

Customer Contacts

Phone
4108500333