FDA UDI In Commercial Distribution 🇺🇸 United States

Geniant Cranial

DI: 08800050902307 · Model: MN30-CRAB025 · KOH YOUNG TECHNOLOGY INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Geniant Cranial
Primary DI
08800050902307
Version / Model
MN30-CRAB025
Company Name
KOH YOUNG TECHNOLOGY INC.
Labeler DUNS
695406977
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-20
Public Version
1
Public Version Date
2025-02-28
Public Version Status
New
Public Device Record Key
e14201ce-ab3c-401d-9fc8-91b7cea6a6a7

Device Description

RTD 2.5 mm Bushing 02

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
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
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
HAW Neurological Stereotaxic Instrument

GMDN Terms

Code Name
32568 Neurological stereotactic surgery system

Identifiers

Type ID
Primary 08800050902307

Premarket Submissions

Submission Number Supplement Number
K241333 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 2.5 Millimeter