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 |