Primary Device ID | 06950715503263 |
NIH Device Record Key | 0695b475-5631-47b6-b6ee-5bf1faa6a5e1 |
Commercial Distribution Discontinuation | 2030-04-27 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | cofoecare |
Version Model Number | KF-WBY-01 |
Company DUNS | 544425204 |
Company Name | Cofoe Medical Technology Co.,Ltd |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06950715503263 [Primary] |
DWL | Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-22 |
Device Publish Date | 2024-07-12 |
06950715503263 | Compression stocking |
06950715503256 | Compression stocking |
06950715503249 | Compression stocking |
06950715503232 | Compression stocking |
06950715503225 | Compression stocking |
06950715503218 | Compression stocking |
06950715503201 | Compression stocking |
06950715503195 | Compression stocking |
06950715503188 | Compression stocking |
06950715503171 | Compression stocking |