Primary Device ID | 00884450780138 |
NIH Device Record Key | 117789fb-ca58-4ede-b056-d78484b005a1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arcadia™ |
Version Model Number | F |
Catalog Number | ARC30SB |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450780138 [Primary] |
HRX | Arthroscope |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-11 |
Device Publish Date | 2024-11-02 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ARCADIA 98301387 not registered Live/Pending |
Coffee Talks Inc. 2023-12-06 |
ARCADIA 98250656 not registered Live/Pending |
Rep Fitness LLC 2023-11-01 |
ARCADIA 98188757 not registered Live/Pending |
Arcadia Vacation Resort, LLC 2023-09-20 |
ARCADIA 97899130 not registered Live/Pending |
Sportspower Limited 2023-04-20 |
ARCADIA 97867419 not registered Live/Pending |
Arcadia Cold, LLC 2023-03-31 |
ARCADIA 97867346 not registered Live/Pending |
Arcadia Cold, LLC 2023-03-31 |
ARCADIA 97430415 not registered Live/Pending |
MCDM Productions, LLC 2022-05-26 |
ARCADIA 97259568 not registered Live/Pending |
Snap Inc. 2022-02-09 |
ARCADIA 97169707 not registered Live/Pending |
Arcadia Tractor Corp. 2021-12-13 |
ARCADIA 97169522 not registered Live/Pending |
Arcadia Tractor Corp. 2021-12-13 |
ARCADIA 97129213 not registered Live/Pending |
DELTA FAUCET COMPANY 2021-11-17 |
ARCADIA 90821586 not registered Live/Pending |
Shenzhen Jiefeng Investment Co., Ltd. 2021-07-10 |