| Primary Device ID | 00815137022227 |
| NIH Device Record Key | 3d8cbb58-e9ec-4e1c-b79c-296f33dec616 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CaraClip |
| Version Model Number | 431S |
| Company DUNS | 001157841 |
| Company Name | Beekley Corporation |
| 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 | 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00815137022227 [Primary] |
| MDM | Instrument, Manual, Surgical, General Use |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-11-21 |
| Device Publish Date | 2023-11-13 |
| 10815137022224 | Wire protector |
| 00815137022227 | Wire protector |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CARACLIP 97894773 not registered Live/Pending |
Beekley Corporation 2023-04-18 |