Primary Device ID | 06972314460952 |
NIH Device Record Key | cc5a8d1b-85ae-43a0-b6f9-850bbe454b2a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | XTCERA |
Version Model Number | XT-E 98×16 A4 |
Company DUNS | 547044326 |
Company Name | SHENZHEN XIANGTONG 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 | true |
Serial Number | false |
Manufacturing Date | false |
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 | 06972314460952 [Primary] |
EIH | Powder, Porcelain |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-08 |
Device Publish Date | 2023-11-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() XTCERA 97734355 not registered Live/Pending |
SHENZHEN XIANGTONG CO., LTD 2022-12-28 |
![]() XTCERA 97734343 not registered Live/Pending |
SHENZHEN XIANGTONG CO., LTD 2022-12-28 |
![]() XTCERA 97734339 not registered Live/Pending |
SHENZHEN XIANGTONG CO., LTD 2022-12-28 |