| Primary Device ID | 06972615108003 |
| NIH Device Record Key | 24b1428f-ded8-4a25-a421-ae4dbef22312 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | icanclave |
| Version Model Number | 2545D |
| Company DUNS | 421288451 |
| Company Name | Ningbo Ican Machines 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 | 06972615108003 [Primary] |
| FLE | Sterilizer, Steam |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-12-29 |
| Device Publish Date | 2025-12-19 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ICANCLAVE 90741140 not registered Live/Pending |
Ningbo Ican Machines Co., Ltd. 2021-05-28 |