Primary Device ID | 10801741222563 |
NIH Device Record Key | d055fa4f-43ea-4f8d-b03c-8dd2c880ebd0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Prevue II Peripheral Vascular Access System |
Version Model Number | 9770705 |
Catalog Number | 9770705 |
Company DUNS | 044611812 |
Company Name | Bard Access Systems, Inc. |
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 | 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741222566 [Primary] |
GS1 | 10801741222563 [Package] Contains: 00801741222566 Package: CA [25 Units] In Commercial Distribution |
ITX | Transducer, ultrasonic, diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-08-25 |
Device Publish Date | 2021-08-17 |
00801741215049 | BD Prevue II Battery |
00801741215032 | BD Prevue II Power Supply |
00801741215025 | BD Prevue II Cord Wrap |
00801741215018 | BD Prevue II Cue Magnetizer |
00801741215001 | BD Prevue II Probe Holder |
00801741214998 | BD Prevue II Roll Stand |
00801741214981 | BD Prevue II Vascular Access Probe (Refurbished) |
00801741214974 | BD Prevue II Vascular Access Probe |
00801741214967 | BD Prevue II Traditional Probe (Refurbished) |
00801741214950 | BD Prevue II Traditional Probe |
00801741214929 | BD Prevue II Console (Refurbished) |
00801741214912 | BD Prevue II Console |
10801741222563 | BD Prevue II Magnetizer Cover |