Primary Device ID | 00699753531567 |
NIH Device Record Key | 1965dc78-fea2-4c1f-9226-793516b0b2f2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cardiovascular Procedure Kit |
Version Model Number | 72149-02 |
Company DUNS | 177655466 |
Company Name | Terumo Cardiovascular Systems Corporation |
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 | 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00699753531567 [Primary] |
GCJ | Laparoscope, General & Plastic Surgery |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-06 |
Device Publish Date | 2024-05-29 |
50699753509790 | 66774 |
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