Primary Device ID | 10841912106896 |
NIH Device Record Key | d74f8e0a-0e77-4b8d-86d1-adac8973a8fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sterile Single-Use Multi-Angle Needle Guide-Probe Cover Kit |
Version Model Number | 5363 |
Catalog Number | 5363 |
Company DUNS | 965417181 |
Company Name | PROTEK MEDICAL PRODUCTS, 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 | 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 | 00841912106899 [Primary] |
GS1 | 10841912106896 [Package] Contains: 00841912106899 Package: [24 Units] In Commercial Distribution |
ITX | Transducer, Ultrasonic, Diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-25 |
Device Publish Date | 2021-05-17 |
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