| Primary Device ID | 04250381801901 |
| NIH Device Record Key | 7694a4bc-ce0d-4c93-b8d5-c368d51825e0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | House suction cannula, Luer-Lock |
| Version Model Number | 10-308-10 |
| Catalog Number | 10-308-10 |
| Company DUNS | 332893028 |
| Company Name | Spiggle & Theis Medizintechnik 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04250381801901 [Primary] |
| JZF | TUBE, EAR SUCTION |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
[04250381801901]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-15 |
| Device Publish Date | 2023-06-07 |
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