| Primary Device ID | 30801741128883 |
| NIH Device Record Key | 1109bd3b-1e27-4f67-9875-f20f6fa7c30a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pinpoint GT |
| Version Model Number | 9770643 |
| Catalog Number | 9770643 |
| 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 | 3 Inch |
| Length | 3 Inch |
| Length | 3 Inch |
| Length | 3 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00801741128882 [Primary] |
| GS1 | 10801741128889 [Package] Contains: 00801741128882 Package: CA [20 Units] In Commercial Distribution |
| GS1 | 30801741128883 [Package] Contains: 10801741128889 Package: BX [4 Units] In Commercial Distribution |
| PVZ | Non-stainless steel needle |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-23 |
| 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 |