Primary Device ID | 16974795050131 |
NIH Device Record Key | d800cfc8-0079-47ab-90e1-3ce711696b01 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | Sterile |
Company DUNS | 724981491 |
Company Name | Henan Maidingkang 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 | true |
Lot Batch | true |
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 | 06974795050134 [Primary] |
GS1 | 16974795050131 [Package] Contains: 06974795050134 Package: [10 Units] In Commercial Distribution |
PFP | Silicone Hydrogel For Scar Management |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-13 |
Device Publish Date | 2022-06-03 |
06974795056235 - MEDLOT | 2024-11-27 |
06974795053081 - LotFancy | 2024-10-29 |
06974795054835 - LotFancy | 2024-10-28 |
06974795059182 - LotFancy | 2024-09-03 |
06974795052169 - LotFancy | 2024-08-26 |
06974795054194 - LotFancy | 2024-08-26 |
06974795055658 - LotFancy | 2024-08-26 |
06974795052824 - MEDLOT | 2024-07-24 |