Primary Device ID | 00840117329744 |
NIH Device Record Key | 5e5be78d-b8c2-4d91-b439-0568401f4016 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LabChoice Mechanical Pipette, Single Channel, Adjustable Volume 0.5 - 5 ML |
Version Model Number | 40121 |
Company DUNS | 008124539 |
Company Name | Dynarex Corporation |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840117329744 [Primary] |
GS1 | 00840117330948 [Package] Package: Shipper [50 Units] In Commercial Distribution |
JRC | Micro Pipette |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-06-09 |
Device Publish Date | 2025-05-30 |
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