Primary Device ID | 00656204000218 |
NIH Device Record Key | 4665263e-e084-44bf-819e-f7bf62d56b65 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HARNESS PAVLIK TYPE |
Version Model Number | 51968/NA/MD |
Company DUNS | 056007248 |
Company Name | ALIMED, INC. |
Device Count | 1 |
DM Exempt | true |
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 | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com | |
Phone | +1(781)329-2900 |
customerservice@alimed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00656204000218 [Primary] |
IQZ | HAND, EXTERNAL LIMB COMPONENT, 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 | 2022-12-09 |
Device Publish Date | 2022-12-01 |
00656204006142 | 51968/NA/XS |
00656204000232 | 51968/NA/XL |
00656204000225 | 51968/NA/SM |
00656204000218 | 51968/NA/MD |
00656204000201 | 51968/NA/LG |