Primary Device ID | 06977488690013 |
NIH Device Record Key | 30bc33b5-787c-47c1-b299-dcfc1f115d88 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | YiFang |
Version Model Number | YF-002 |
Company DUNS | 551059828 |
Company Name | SHENZHEN YIFANG BLISTER PACKAGING 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 | false |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06977488690013 [Primary] |
FLL | Thermometer, Electronic, Clinical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-09-09 |
Device Publish Date | 2024-08-30 |
06977488690013 | YF-002 |
06977488690006 | YF-001 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
YIFANG 79041065 3427189 Dead/Cancelled |
SHENZHEN YIFANG DIGITAL; TECHNOLOGIES CO., LTD 2007-05-18 |