Primary Device ID | 06970623200092 |
NIH Device Record Key | 67fe3872-d73d-4be6-9a10-c6b85d5aa407 |
Commercial Distribution Discontinuation | 2021-10-08 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Maxcon Sharps Container |
Version Model Number | MA1321 |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06970623200092 [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 | 2021-10-18 |
Device Publish Date | 2021-10-08 |
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