Primary Device ID | 08800016903720 |
NIH Device Record Key | a0bd40df-1ea7-4cbe-ad2e-b6b8342a11be |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Secret PRO Needle Hanpdiece |
Version Model Number | FRX-C2 |
Company DUNS | 689842183 |
Company Name | CLASSYS Inc. |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800016903720 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-08 |
Device Publish Date | 2024-10-31 |
08800016905366 - VOLNEWMER S tip | 2025-06-24 |
08800016905373 - VOLNEWMER V tip | 2025-06-24 |
08800016905380 - VOLNEWMER F tip | 2025-06-24 |
08800016905397 - VOLNEWMER I tip | 2025-06-24 |
08800016905403 - VOLNEWMER S tip(D) | 2025-06-24 |
08800016905410 - VOLNEWMER V tip(D) | 2025-06-24 |
08800016905427 - VOLNEWMER F tip(D) | 2025-06-24 |
08800016905434 - VOLNEWMER I tip(D) | 2025-06-24 |