Micro ear forceps 34-0254

GUDID 04250676734860

oval cups, straight, extrafine shaft 1.5 mm, 0.5x1.0 mm, 8 cm

Spiggle & Theis Medizintechnik GmbH

Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable Surgical soft-tissue manipulation forceps, alligator, reusable
Primary Device ID04250676734860
NIH Device Record Key003bddf5-642d-4977-bbb3-0cd017ddabbc
Commercial Distribution StatusIn Commercial Distribution
Brand NameMicro ear forceps
Version Model Number34-0254
Catalog Number34-0254
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
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104250676734860 [Primary]

FDA Product Code

LRCINSTRUMENT, ENT MANUAL SURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


[04250676734860]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-21
Device Publish Date2023-08-11

On-Brand Devices [Micro ear forceps]

04250676715937oval cups, curved downwards, fine shaft 1.8 mm, 0.8x1.3 mm, 8 cm
04250676715920oval cups, curved upwards, super fine shaft 1.3 mm, 0.5x1.0 mm, 8 cm
04250676703200oval cups, curved downwards, fine 0.8x1.3 mm, shaft 1.8 mm, 8 cm
04250381869161oval cups, curved upwards, super fine shaft 1.3 mm, 0.5x1.0 mm, 8 cm
04250381854099oval cups, straight, superfine shaft 1,3 mm, 0.5x1.0 mm, 8 cm
04250381854082oval cups, straight, extrafine shaft 1.5 mm, 0.5x1.0 mm, 8 cm
04250381854051oval cups, curved right, fine 0.8x1.3 mm, 8 cm, black coated
04250381849637oval cups, straight, fine 0.8x1.3 mm, 8 cm
04250381848647oval cups, straight, superfine shaft 1.3 mm, 0.5x1.0 mm, 8 cm
04250381848630oval cups, straight, extra fine shaft 1.5 mm, 0.5x1.0 mm, 8 cm
04250381848623oval cups, curved upwards, fine 0.8x1.3 mm, 8 cm
04250381848616oval cups, left curved, fine 0.8x1.3 mm, 8 cm
04250381848609oval cups, curved right, fine 0.8x1.3 mm, 8 cm
04250676734877oval cups, curved downwards, fine 0.8x1.3 mm, shaft 1.8 mm, 8 cm
04250676734853oval cups, curved upwards, fine 0.8x1.3 mm, 8 cm
04250676734860oval cups, straight, extrafine shaft 1.5 mm, 0.5x1.0 mm, 8 cm

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