Primary Device ID | 07613327424140 |
NIH Device Record Key | 0c04f0e7-f0b0-4c8b-829e-bd10d2894e83 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProForm |
Version Model Number | 2815 |
Catalog Number | 281505550005 |
Company DUNS | 078470558 |
Company Name | STRYKER CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Handling Environment Temperature | Between -40 Degrees Celsius and 60 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327424140 [Primary] |
IKY | MATTRESS, FLOTATION THERAPY, NON-POWERED |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-05-28 |
Device Publish Date | 2019-05-20 |
07613327424164 | 2815 |
07613327424133 | 2815 |
07613327424157 | 2815 |
07613327424140 | 2815 |
07613327424119 | 2815 |
07613327424102 | 2815 |
07613327424065 | 2815 |
07613327485813 | 2815 |