Primary Device ID | 00857268006424 |
NIH Device Record Key | 6ef81eda-9952-43f1-9a4d-46a1a04d6d38 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dolphin Fluid Immersion Simulation |
Version Model Number | DLPH-3582LPOOOJ-M |
Catalog Number | DLPH-3582LPOOOJ-M |
Company DUNS | 790937150 |
Company Name | JOERNS HEALTHCARE, LLC |
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 | true |
Serial Number | false |
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 | 800-826-0270 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00857268006424 [Primary] |
FNM | Mattress, Air Flotation, Alternating Pressure |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-02 |
00857268006738 | DLPH-3582NCOOJ-M |
00857268006721 | DLPH-4282NCOOJ-M |
00857268006714 | DLPH-4882OOOOJ-M |
00857268006479 | DLPH-4882OOOOJ-M |
00857268006462 | DLPH-4282NCOOJ-M |
00857268006455 | DLPH-4282LPOOJ-M |
00857268006448 | DLPH-4282OOOOJ-M |
00857268006431 | DLPH-3582NCOOJ-M |
00857268006424 | DLPH-3582LPOOOJ-M |
00857268006417 | DLPH-3582OOOOJ-M |
00857268006400 | DLPH-1717WCOOJ-C |
00857268006394 | FIS Stretcher |
00857268006318 | DLPH-4282OOOOJ-M |
00857268006271 | DLPH-3582OOOOJ-M |
00857268006257 | FIS Step-deck |
00810055880171 | MATTRESS, DOLPHIN,35X92X8,NSC, |