Primary Device ID | 10641043885017 |
NIH Device Record Key | 1a6aebbd-dfcf-45f4-835a-00bfcb255d3d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hand Pump Assembly |
Version Model Number | 88-GCT501 |
Company DUNS | 032705659 |
Company Name | MERCURY ENTERPRISES, 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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10641043885017 [Primary] |
KNT | Tubes, Gastrointestinal (And Accessories) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-23 |
Device Publish Date | 2023-06-15 |
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30641043913653 - Neo-Tee T-Piece Resuscitator Circuit | 2024-02-16 |
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10641043885017 - Hand Pump Assembly | 2023-06-23 |
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30641043564343 - CPR-2 Bag | 2023-04-12 |
30641043566026 - CPR-2 Bag | 2023-03-17 |
30641043564572 - CPR-2 Bag | 2022-08-10 |