| Primary Device ID | 04250337120384 |
| NIH Device Record Key | 9dcfa8d9-c776-4497-8fb4-1173513bf520 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Working Tube |
| Version Model Number | WTS709304 |
| Catalog Number | WTS709304 |
| 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 |
| 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 | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com | |
| Phone | +497212551407010 |
| info@joimax.com |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04250337120384 [Primary] |
| GDF | Guide, Needle, Surgical |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
[04250337120384]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-10-09 |
| Device Publish Date | 2023-09-29 |
| 04250337120384 | Working Tube with sealing, straight 90° |
| 04250337120377 | Working Tube with sealing, Standard Lip |
| 04250337120360 | Working Tube with sealing, straight 90° |
| 04250337120353 | Working Tube with sealing, Standard Lip |