Primary Device ID | 06970623200023 |
NIH Device Record Key | d82731e0-b666-4e2a-8e55-729cdacf449e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Maxcon Sharps Container |
Version Model Number | MA1341 |
Company DUNS | 544557314 |
Company Name | NINGBO MAXCON MEDICAL TECHNOLOGY CO., LTD. |
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 | 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 | 06970623200023 [Primary] |
MMK | Container, Sharps |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-08-11 |
Device Publish Date | 2021-08-03 |
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