Primary Device ID | 30801741128876 |
NIH Device Record Key | aed3800b-7318-43a0-981b-2d7907ddc6b8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pinpoint GT |
Version Model Number | 9770642 |
Catalog Number | 9770642 |
Company DUNS | 044611812 |
Company Name | Bard Access Systems, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)545-0890 |
medical.services@crbard.com | |
Phone | +1(800)545-0890 |
medical.services@crbard.com |
Length | 2.75 Inch |
Length | 2.75 Inch |
Length | 2.75 Inch |
Length | 2.75 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741128875 [Primary] |
GS1 | 10801741128872 [Package] Contains: 00801741128875 Package: CA [20 Units] In Commercial Distribution |
GS1 | 30801741128876 [Package] Contains: 10801741128872 Package: BX [4 Units] In Commercial Distribution |
BSP | NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-10-04 |
30801741128937 | Hypodermic Pinpoint GT Needle |
30801741128920 | Hypodermic Pinpoint GT Needle |
10801741128919 | Pinpoint GT Needle |
10801741128902 | Hypodermic Pinpoint GT Needle |
30801741128890 | Pinpoint GT Needle |
30801741128883 | Hypodermic Pinpoint GT Needle |
30801741128876 | Pinpoint GT Needle |
30801741128869 | Pinpoint GT Needle |
30801741128852 | Pinpoint GT Needle |