Ambu

GUDID 08718375869352

Probe Hooked Triple 37x0.75mm 1pc

Technomed Engineering B.V.

Nerve-locating system probe, single-use
Primary Device ID08718375869352
NIH Device Record Key970e6d9a-a726-49f1-88e5-f98fdabc3f50
Commercial Distribution StatusIn Commercial Distribution
Brand NameAmbu
Version Model Number73605-190/1
Company DUNS418415568
Company NameTechnomed Engineering B.V.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl
Phone+31434086868
Emailinfo@technomed.nl

Device Identifiers

Device Issuing AgencyDevice ID
GS108718375869338 [Primary]
GS108718375869352 [Package]
Contains: 08718375869338
Package: Pouch [1 Units]
In Commercial Distribution

FDA Product Code

GXZElectrode, Needle

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-07-12
Device Publish Date2022-07-04

On-Brand Devices [Ambu]

08718375869352Probe Hooked Triple 37x0.75mm 1pc
08718375869321Probe Hooked Double 37x0.75mm 1pc
08718375869291Disposable Subdermal Needle, corkscrew 2.5m twisted wire 12pairs & PC
08718375869260Disposable Subdermal Needle, corkscrew 2.0m twisted wire 12pairs & PC
08718375869239Disposable Subdermal Needle, corkscrew 1.2m twisted wire 12pairs & PC
08718375869208Disposable Subdermal Needle Electrode, curved 2m wire 5x5 colors 25pcs
08718375869178Disposable Subdermal Needle Electrode, curved 1.5m wire 5x5 colors 25pcs
08718375869147Disposable Subdermal Needle Electrode, hooked 2.5m wire 4x6 colors 24pcs
08718375869116Disposable Subdermal Needle Electrode, hooked 2m wire 4x6 colors 24pcs
08718375869086Disposable Subdermal Needle Electrode, hooked 1.2m wire 4x6 colors 24pcs
08720791370886Ambu® Subdermal Corkscrew 2.5m wire 4x6 colors 24pcs
08720791370855Ambu® Subdermal Corkscrew 2.0m wire 4x6 colors 24pcs
08720791370817Ambu® Subdermal Corkscrew 1.2m wire 4x6 colors 24pcs
08718375869253Ambu® Subdermal Twisted Pair Corkscrew 2.0m twisted wire 12pairs & PC
08718375869222Ambu® Subdermal Twisted Pair Corkscrew 1.2m twisted wire 12pairs & PC

Trademark Results [Ambu]

Mark Image

Registration | Serial
Company
Trademark
Application Date
AMBU
AMBU
98192535 not registered Live/Pending
AMBU A/S
2023-09-22
AMBU
AMBU
90002202 not registered Live/Pending
AMBU
2020-06-15
AMBU
AMBU
79051291 3554442 Live/Registered
AMBU A/S
2008-02-15
AMBU
AMBU
74156351 1686178 Live/Registered
AMBU A/S
1991-04-12
AMBU
AMBU
73438330 1330624 Dead/Cancelled
Testa-Laboratorium A/S
1983-08-08
AMBU
AMBU
73023700 1040868 Dead/Expired
TESTA-LABORATORIUM A/S
1974-06-10
AMBU
AMBU
72127671 0740102 Dead/Cancelled
Testa Laboratorium A/S
1961-09-11
AMBU
AMBU
72055090 0705020 Dead/Cancelled
TESTA LABORATORIUM A/S
1958-07-10

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