Primary Device ID | 16959180703915 |
NIH Device Record Key | 5d1bfab0-0fb6-4cbf-b10e-790beb0beddb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pediatric Flex Tubing |
Version Model Number | VR018 |
Company DUNS | 420798349 |
Company Name | VR Medical 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 | true |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 16959180703915 [Primary] |
BZO | Set, Tubing And Support, Ventilator (W Harness) |
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 | 2018-02-07 |
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16959180753194 - VR Medical Technology Co., Ltd. | 2024-08-27 Closed suction System ,VR041607 |
16959180703731 - Closed Suction System | 2020-05-14 |
16959180704219 - Closed Suction System | 2020-05-14 |
16959180704318 - Closed Suction System | 2020-05-14 |
16959180704332 - Closed Suction System | 2020-05-14 |