FDA.reportPublic FDA data

icotec instrument, Cervical Cage, Container Rack

Primary DI
07640164846460
Brand
icotec instrument, Cervical Cage, Container Rack
Company
icotec AG
Model
41-22-3
Catalog number
41-22-3
Device description
icotec instrument, Cervical Cage, Container Rack
Published
2022-08-29
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
ODPIntervertebral Fusion Device With Bone Graft, Cervical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
ODPIntervertebral Fusion Device With Bone Graft, CervicalOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07640164846460PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07640164846460076401648464607640164846460

GMDN Terms#

Term, Definition table
TermDefinition
Sterilization/disinfection container, reusableA receptacle designed to hold wrapped and/or unwrapped medical/dental devices in a chemical washer/disinfector and/or sterilizer during the washing/disinfection and/or sterilization cycle(s). It may be designed as a tray to allow full or partial immersion of the devices in a liquid disinfectant, or as an enclosed box to prevent contamination once the sterilization process is finished. The container may also be used for transport and storage of the processed devices, and may have features such as an expiry date label, breathing filter, built-in slots or inserts to hold instruments, and stacking capabilities. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+41717570000info@icotec.ch

Regulatory Flags#

DUNS number
480789465
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

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Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
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07640172552575CMORE® System, Drill Guide Stop45-030-145-030-12025-11-24
07640172552582CMORE® System, Drill Bit, Ø 2.3 mm45-04045-0402025-11-24
07640172552599CMORE® System, Feeler45-07045-0702025-11-24
07640172552605CMORE® System, In-line Handle, AO Coupling45-10045-1002025-11-24
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07640172552629CMORE® System, Solid Tap, Ø 4.0 mm 45-14045-1402025-11-24
07640172552636CMORE® System, Solid Tap, Ø 4.5 mm45-14545-1452025-11-24
07640172552643CMORE® System, Screwdriver Shaft, T1545-21045-2102025-11-24
07640172552650CMORE® System, Tulip Aligner 45-22045-2202025-11-24
07640172552674CMORE® System, Template for Rods CT1, CT2, R12045-24045-2402025-11-24
07640172552681CMORE® System, Rod Cutter 45-25045-2502025-11-24
07640172552698CMORE® System, French Rod Bender 45-26045-2602025-11-24
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07640172552759CMORE® System, Solid Tap, Ø 5.0 mm45-15045-1502025-11-24

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