| Primary Device ID | 20813079020305 |
| NIH Device Record Key | bdb757e7-b585-4892-b73d-49ae9144991b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Guidewire Introducer Needle |
| Version Model Number | GWI-1802 |
| Catalog Number | GWI-1802 |
| Company DUNS | 788472314 |
| Company Name | REMINGTON MEDICAL, INC. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com | |
| Phone | +1(800)989-0057 |
| Quality@Remmed.com |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Needle Gauge | 18 Gauge |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813079020301 [Primary] |
| GS1 | 10813079020308 [Package] Contains: 00813079020301 Package: Inner Carton [10 Units] In Commercial Distribution |
| GS1 | 20813079020305 [Package] Contains: 10813079020308 Package: Shipping Carton [10 Units] In Commercial Distribution |
| DWS | INSTRUMENTS, SURGICAL, CARDIOVASCULAR |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
[20813079020305]
Ethylene Oxide
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-02 |
| Device Publish Date | 2020-09-24 |
| 20813079020336 | 19ga (1.1mm) x 7 cm |
| 20813079020305 | 18ga (1.3mm) x 7cm |