Phoenix
GUDID 44900719326016
DR.JAPAN CO., LTD.
Epidural needle, non-threaded Epidural needle, non-threaded| Primary Device ID | 44900719326016 |
| NIH Device Record Key | 4ad98da2-76fa-45e3-904b-746f800f0284 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Phoenix |
| Version Model Number | TUFW16G350 |
| Company DUNS | 701082349 |
| Company Name | DR.JAPAN CO., LTD. |
| Device Count | 100 |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Device Dimensions
| Length | 3.5 Inch |
| Needle Gauge | 16 Gauge |
| Length | 3.5 Inch |
| Needle Gauge | 16 Gauge |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04900719326018 [Unit of Use] |
| GS1 | 44900719326016 [Primary] |
FDA Product Code
| BSP | Needle, Conduction, Anesthetic (W/Wo Introducer) |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[44900719326016]
Ethylene Oxide
[44900719326016]
Ethylene Oxide
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-24 |
On-Brand Devices [Phoenix]
Trademark Results [Phoenix]
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.