Primary Device ID | 16970729040025 |
NIH Device Record Key | b6b07a06-c786-44f6-bf32-f479c8b78603 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TeleRPM™ |
Version Model Number | GBS-2104-G |
Company DUNS | 544411562 |
Company Name | Zhongshan Transtek Electronics 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 | false |
Serial Number | true |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 16970729040025 [Primary] |
FRI | Scale, Stand-On, Patient |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-07 |
Device Publish Date | 2022-11-29 |
16970729040025 | GBS-2104-G |
16970729040018 | GBS-2104-G |
06970729040103 | GBS-2104-G |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TELERPM 97521185 not registered Live/Pending |
Guangdong Transtek Medical Electronics Co., Ltd. 2022-07-26 |