FDA UDI In Commercial Distribution 🇺🇸 United States

icotec Systems, Fixation device

DI: 07640172553855 · Model: 42-893 · icotec AG
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
icotec Systems, Fixation device
Primary DI
07640172553855
Version / Model
42-893
Catalog Number
42-893
Company Name
icotec AG
Labeler DUNS
480789465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-13
Public Version
2
Public Version Date
2025-11-18
Public Version Status
Update
Public Device Record Key
13269d72-5703-4a79-b787-ee58203d326d

Device Description

icotec Systems, Fixation device

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NKG Posterior Cervical Screw System
OLO Orthopedic Stereotaxic Instrument
NKB Thoracolumbosacral Pedicle Screw System
PML Bone Cement, Posterior Screw Augmentation

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 07640172553855

Customer Contacts

Phone
+41717570000