Primary Device ID | 00815962020214 |
NIH Device Record Key | 61d31ddb-0f30-4734-9e8c-092b9d116a39 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bioness Integrated System (BITS) Mobile Configuration |
Version Model Number | BIT-2224 |
Company DUNS | 182287727 |
Company Name | BIONESS INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)211-9136 |
info@bioness.com | |
Phone | +1(800)211-9136 |
info@bioness.com | |
Phone | +1(800)211-9136 |
info@bioness.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815962020214 [Primary] |
IKK | SYSTEM, ISOKINETIC TESTING AND EVALUATION |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-07-10 |
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