Primary Device ID | 30748426118572 |
NIH Device Record Key | 9242f82d-06a2-4f20-b169-7b025c5c1aae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Skytron Argos |
Version Model Number | B5-010-02-1 |
Company DUNS | 106908437 |
Company Name | Microtek Medical Inc. |
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 | true |
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 | 00748426118571 [Primary] |
GS1 | 30748426118572 [Package] Contains: 00748426118571 Package: [25 Units] In Commercial Distribution |
GS1 | 50748426118576 [Package] Package: [2 Units] In Commercial Distribution |
PUI | Drape, Surgical, Exempt |
Steralize Prior To Use | true |
Device Is Sterile | true |
[30748426118572]
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Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-16 |
Device Publish Date | 2022-08-08 |
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