icotec Instrument Ring Curette 38-031-00

GUDID 07640164841755

icotec Instrument Ring Curette

icotec AG

Spinal curette Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use
Primary Device ID07640164841755
NIH Device Record Key0a503d54-9494-41f0-aec5-55170dfdd848
Commercial Distribution StatusIn Commercial Distribution
Brand Nameicotec Instrument Ring Curette
Version Model Number38-031-00
Catalog Number38-031-00
Company DUNS480789465
Company Nameicotec AG
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch

Device Identifiers

Device Issuing AgencyDevice ID
GS107640164841755 [Primary]

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

[07640164841755]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-09-06
Device Publish Date2018-07-16

Devices Manufactured by icotec AG

07640164846675 - VADER Pedicle System MIS, Rod, Carbon/PEEK, Straight, Ø 6.0 r000 x 30 mm2024-04-04 VADER Pedicle System MIS, Rod, Carbon/PEEK, Straight, Ø 6.0 r000 x 30 mm
07640164846804 - VADER Pedicle System MIS, Rod, Carbon/PEEK, Curved, Ø 6.0 r120 x 30 mm2024-04-04 VADER Pedicle System MIS, Rod, Carbon/PEEK, Curved, Ø 6.0 r120 x 30 mm
07640164846880 - VADER Pedicle System MIS, Rod, Carbon/PEEK, Curved, Ø 6.0 r450 x 30 mm2024-04-04 VADER Pedicle System MIS, Rod, Carbon/PEEK, Curved, Ø 6.0 r450 x 30 mm
07640164848785 - icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 35 mm2024-04-04 icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 35 mm
07640164848792 - icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 40 mm2024-04-04 icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 40 mm
07640164848808 - icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 45 mm2024-04-04 icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 45 mm
07640164848815 - icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 50 mm2024-04-04 icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 50 mm
07640164848822 - icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 55 mm2024-04-04 icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 55 mm
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