Primary Device ID | 06970544023879 |
NIH Device Record Key | 0bb057bb-84b4-4b28-b979-989ef4b8fb94 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | XTCERA |
Version Model Number | 18*15*13 A1 |
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 | 06970544023879 [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 |