| Primary Device ID | 04250381891957 |
| NIH Device Record Key | 0696acd7-6e72-49f4-b7e2-1e337fb25e02 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Metal bowl |
| Version Model Number | 80-501-02 |
| Catalog Number | 80-501-02 |
| 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 | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04250381891957 [Primary] |
| LRC | INSTRUMENT, ENT MANUAL SURGICAL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
[04250381891957]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-16 |
| Device Publish Date | 2023-08-08 |
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