Primary Device ID | 00841912105649 |
NIH Device Record Key | 8fe639fb-0bad-46b3-ab13-cf126afc2e78 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Multi-Angle Biopsy Starter Kit |
Version Model Number | 7265 |
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 | true |
Device Combination Product | false |
Single Use | false |
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 | 00841912105649 [Primary] |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841912105649]
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[00841912105649]
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Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-12-23 |
Device Publish Date | 2018-07-13 |
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