Primary Device ID | 00884838100213 |
NIH Device Record Key | 887c048e-7d51-48fe-b59f-ff4a89585572 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Transducer C5-1 |
Version Model Number | 989606714071 |
Company DUNS | 063377717 |
Company Name | Philips Ultrasound LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838100213 [Primary] |
IYN | System, Imaging, Pulsed Doppler, Ultrasonic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-07 |
Device Publish Date | 2024-07-30 |
00884838100213 - Transducer C5-1 | 2024-08-07Introduction of C5-1 (Shanghai Version) to rest of the world. |
00884838100213 - Transducer C5-1 | 2024-08-07 Introduction of C5-1 (Shanghai Version) to rest of the world. |
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