Primary Device ID | 00817012029345 |
NIH Device Record Key | b3559a02-edb6-422e-81e7-a9cab651a089 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | K-2SM SmartMatt |
Version Model Number | K-2SM-B42-8 |
Catalog Number | K-2SM-B42-8 |
Company DUNS | 135241342 |
Company Name | KAP MEDICAL |
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 | true |
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 |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com | |
Phone | 951-340-4360 |
sales@kapmedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817012029345 [Primary] |
FNM | Mattress, Air Flotation, Alternating Pressure |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-21 |
Device Publish Date | 2020-08-13 |
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