| Primary Device ID | 07290018896037 |
| NIH Device Record Key | bf8e1e2f-93e7-4dfe-9b58-2fcb5bf52c6c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SU-VEID |
| Version Model Number | 18103100 |
| Catalog Number | 18103100 |
| Company DUNS | 600634887 |
| Company Name | ANGIE TECHNOLOGIES LTD |
| 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 | true |
| 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 | 07290018896037 [Primary] |
| FMF | Syringe, Piston |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
[07290018896037]
Ethylene Oxide
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-05-31 |
| Device Publish Date | 2021-05-23 |
| 07290018896235 | Carton of 16 boxes (DI# 07290018896136) of 30 SU-VEID units each (DI# 07290018896037) - for a to |
| 07290018896136 | Package of 30 SU-VEID units (DI# 07290018896037) |
| 07290018896037 | Vein entry indicator device |