Fisch footplate perforator 10-658-05

GUDID 04250381849507

0.5 mm, 16 cm

Spiggle & Theis Medizintechnik GmbH

Automatic cranial perforator, reusable
Primary Device ID04250381849507
NIH Device Record Key83d824e5-3d97-4da6-ad70-f462abba319b
Commercial Distribution StatusIn Commercial Distribution
Brand NameFisch footplate perforator
Version Model Number10-658-05
Catalog Number10-658-05
Company DUNS332893028
Company NameSpiggle & Theis Medizintechnik GmbH
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104250381849507 [Primary]

FDA Product Code

JYSPERFORATOR, EAR-LOBE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


[04250381849507]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-21
Device Publish Date2022-09-13

On-Brand Devices [Fisch footplate perforator]

042503818495380.8 mm, 16 cm
042503818495140.6 mm, 16 cm
042503818495070.5 mm, 16 cm
042503818494910.4 mm, 16 cm
042503818484490.3 mm, 16 cm
042506767355390.7 mm, 16 cm

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.