Primary Device ID | 06946725527115 |
NIH Device Record Key | af7940a0-4e66-43ac-9947-8748cbbc2bd4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Philips |
Version Model Number | A0003D05 |
Company DUNS | 529691989 |
Company Name | APK Technology Co.,Ltd. |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | 06946725527115 [Primary] |
DSA | Cable, Transducer And Electrode, Patient, (Including Connector) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-08-06 |
Device Publish Date | 2018-07-06 |
06946725527115 | A0003D05 |
06946725529072 | Temperature Adaptter Cable |
06946725528648 | PH-989803171851 |