Primary Device ID | 16971227404920 |
NIH Device Record Key | 9e13d666-dacc-4cb9-98be-effdc31c94ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Microdot |
Version Model Number | HB-100 |
Company DUNS | 421335278 |
Company Name | Promisemed Hangzhou Meditech Co., Ltd. |
Device Count | 50 |
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 | true |
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 | 06971227404923 [Primary] |
GS1 | 16971227404920 [Unit of Use] |
FMK | Lancet, Blood |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-04 |
Device Publish Date | 2021-09-24 |
16971227404920 | HB-100 |
06971227404916 | HB-085 |