| Primary Device ID | 04250381814116 |
| NIH Device Record Key | d456d821-59f9-478d-b1f4-be140d992fa7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kerrison sphenoid punch |
| Version Model Number | 30-473-10 |
| Catalog Number | 30-473-10 |
| 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 | |
| Phone | +492206908165 |
| c.winterschladen@spiggle-theis.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04250381814116 [Primary] |
| LRC | INSTRUMENT, ENT MANUAL SURGICAL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
[04250381814116]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-19 |
| Device Publish Date | 2024-11-11 |
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| 04250676705532 | 40° upw., golden tip, totally detachable 2 mm, 18 cm |
| 04250676705525 | 40° upw., golden tip, totally detachable 1 mm, 18 cm |
| 04250676705501 | 90° upw., golden tip, totally detachable 4 mm, 18 cm |
| 04250676705495 | 90° upw., golden tip, totally detachable 3 mm, 18 cm |
| 04250676705488 | 90° upw., golden tip, totally detachable 2 mm, 18 cm |
| 04250676705471 | 90° upw., golden tip, totally detachable 1 mm, 18 cm |
| 04250381814123 | 40° downw., golden tip, totally detach. 2 mm, 18 cm |
| 04250676725974 | 40° upw., golden tip, totally detachable 1 mm, 20 cm |
| 04250676725561 | 90° upw., golden tip, totally detachable 1 mm, 23 cm |
| 04250381814116 | 40° downw., golden tip, totally detach. 1 mm, 18 cm |