Primary Device ID | 04250381891513 |
NIH Device Record Key | 84b2412c-240f-4b5f-85be-11ab26bb7b12 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Duval tissue forceps |
Version Model Number | 80-405-20 |
Catalog Number | 80-405-20 |
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 | 04250381891513 [Primary] |
LRC | INSTRUMENT, ENT MANUAL SURGICAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
[04250381891513]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-07 |
Device Publish Date | 2022-09-29 |
04250381891513 | straight 15 mm wide, length 20 cm |
04250676744791 | straight 13 mm wide, length 18 cm |