Antmed
GUDID 06945764412543
ShenZhen Antmed Co., Ltd
Radiographic procedure tubing| Primary Device ID | 06945764412543 |
| NIH Device Record Key | af816c54-75ee-4ab1-9c43-d45ade10ae3e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Antmed |
| Version Model Number | HBR200 |
| Company DUNS | 527221254 |
| Company Name | ShenZhen Antmed Co., Ltd |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06945764406740 [Primary] |
| GS1 | 06945764412543 [Package] Contains: 06945764406740 Package: [50 Units] In Commercial Distribution |
| GS1 | 06945764413540 [Package] Package: [4 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K131770
FDA Product Code
| DQO | Catheter, Intravascular, Diagnostic |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-26 |
| Device Publish Date | 2024-04-18 |
On-Brand Devices [Antmed]
Trademark Results [Antmed]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ANTMED 86771799 5062252 Live/Registered |
SHENZHEN ANTMED CO., LTD 2015-09-29 |
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