CESSYS® TNC582820Y
GUDID 04250337116837
CESSYS® Dorsal DIN-Norm-Container, yellow Lid
Joimax GmbH
Device sterilization/disinfection container, reusable| Primary Device ID | 04250337116837 |
| NIH Device Record Key | d8b24a90-583e-41e3-b690-9dda5cb7e9c0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CESSYS® |
| Version Model Number | TNC582820Y |
| Catalog Number | TNC582820Y |
| Company DUNS | 344267187 |
| Company Name | Joimax GmbH |
| Device Count | 1 |
| DM Exempt | false |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04250337116837 [Primary] |
FDA Product Code
| FSM | TRAY, SURGICAL, INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
[04250337116837]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2023-04-04 |
| Device Publish Date | 2022-12-30 |
On-Brand Devices [CESSYS®]
| 04250337114697 | CESSYS® Dorsal FHD Laminoscope (4.7 WCh), combo |
| 04250337114680 | CESSYS® Dorsal FHD Laminoscope (4.7 WCh), ocular |
| 04250337105879 | CESSYS® Cervical Hybrid Scope, combo |
| 04250337116837 | CESSYS® Dorsal DIN-Norm-Container, yellow Lid |
| 04250337108818 | CESSYS® DIN-Norm-Container, gold Lid |
| 04250337105152 | CESSYS® Cervical Reamer |
Trademark Results [CESSYS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CESSYS 79062669 3799655 Live/Registered |
joimax GmbH 2008-10-10 |
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