Primary Device ID | 05055982700429 |
NIH Device Record Key | 117d1233-9819-4de5-a948-ef86b62be058 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FLOWTRON ACS900 |
Version Model Number | 526000-02-P |
Company DUNS | 355804758 |
Company Name | Arjohuntleigh AB |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05055982700429 [Primary] |
JOW | SLEEVE, LIMB, COMPRESSIBLE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-12-16 |
Device Publish Date | 2016-09-23 |
05055982700429 | DVT Prevention Compression Pump - ACS900 PUMP US OR TUBE SET |
05055982700412 | DVT Prevention Compression Pump - ACS900 PUMP US STD TUBE SET |
05055982700405 | DVT Prevention Compression Pump - DVT Prevention Compression Pump - ACS900 PUMP US OR TUBE SET |
05055982700399 | DVT Prevention Compression Pump - ACS900 PUMP US STD TUBE SET |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLOWTRON ACS900 79326321 not registered Live/Pending |
Arjo IP Holding AB 2021-06-30 |