Rochester-Pean artery forceps 80-383-18

GUDID 04250676733016

curved, anatomical 18.5 cm

Spiggle & Theis Medizintechnik GmbH

Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device ID04250676733016
NIH Device Record Key0d2140bd-a0c2-40d5-8195-aca58c498c74
Commercial Distribution StatusIn Commercial Distribution
Brand NameRochester-Pean artery forceps
Version Model Number80-383-18
Catalog Number80-383-18
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
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104250676733016 [Primary]

FDA Product Code

LRCINSTRUMENT, ENT MANUAL SURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


[04250676733016]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-07
Device Publish Date2022-09-29

On-Brand Devices [Rochester-Pean artery forceps]

04250676733030curved, anatomical 22 cm
04250676733023curved, anatomical 20.5 cm
04250676733016curved, anatomical 18.5 cm
04250676733009straight, anatomical 20 cm
04250676732996straight, anatomical 18.5 cm
04250676744739curved, anatomical 22 cm
04250676744722curved, anatomical 20 cm
04250676744715curved, anatomical 18 cm
04250676744708straight, anatomical 20 cm
04250676744692straight, anatomical 18 cm

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.