Primary Device ID | 06946725529072 |
NIH Device Record Key | 7cad0277-9937-440d-b2e7-3d07ac7d1b94 |
Commercial Distribution Discontinuation | 2021-05-28 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Philips |
Version Model Number | DHP-30-AD0 |
Company DUNS | 529691989 |
Company Name | APK Technology Co.,Ltd. |
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 | true |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06946725529072 [Primary] |
IKD | Cable, Electrode |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-06-06 |
Device Publish Date | 2021-05-28 |
06946725527115 | A0003D05 |
06946725529072 | Temperature Adaptter Cable |
06946725528648 | PH-989803171851 |