Primary Device ID | 00815067043682 |
NIH Device Record Key | 68a4c63a-7d5c-460b-a1a7-a1a24fbbb6a5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MERIDIAN |
Version Model Number | X1SAPM201 |
Company DUNS | 827221698 |
Company Name | COMPASS HEALTH BRANDS CORP. |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815067043682 [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 | 2020-09-15 |
Device Publish Date | 2020-09-07 |
00815067043378 | 54'' APM BARIATRIC SYSTEM |
00815067042913 | Ultra Care Excel MRS System |
00815067042661 | 4581 |
00815067043798 | MER-SAPM PUMP - 8 LPM/350 LB CAP |
00815067043743 | MER-SAPM53 MATTRESS ONLY |
00815067043682 | MER-SAPM2 MATTRESS ONLY |