Primary Device ID | 00811746032671 |
NIH Device Record Key | a5a1f1cf-0545-48b8-9e90-8f8c54527ed5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PowerCordGB |
Version Model Number | CRF-PGB |
Catalog Number | CRF-PGB |
Company DUNS | 080897872 |
Company Name | CAMBRIDGE INTERVENTIONAL LLC |
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 | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com | |
Phone | 781-221-5300 |
info@cambint.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00811746032671 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-26 |
Device Publish Date | 2020-10-16 |
00811746033159 - ProcedureKitCRF | 2023-08-08 CRF Procedure Kit |
00811746033166 - ProcedureKitCRF | 2023-08-08 CRF Procedure Kit |
00811746033173 - ProcedureKitCRF | 2023-08-08 CRF Procedure Kit |
00811746033180 - ProcedureKitCRF | 2023-08-08 CRF Procedure Kit |
00811746033197 - ProcedureKitCRF | 2023-08-08 CRF Procedure Kit |
00811746033203 - ProcedureKitCRF | 2023-08-08 CRF Procedure Kit |
00811746033210 - ProcedureKitCRF | 2023-08-08 CRF Procedure Kit |
00811746033227 - ProcedureKitCRF | 2023-08-08 CRF Procedure Kit |