FDA UDI In Commercial Distribution 🇺🇸 United States

CranioFit

DI: M384CF260800160 · Model: KT-T8L15H2 · Bioplate, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CranioFit
Primary DI
M384CF260800160
Version / Model
KT-T8L15H2
Catalog Number
CF26080016
Company Name
Bioplate, Inc.
Labeler DUNS
838734093
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-10
Public Version
2
Public Version Date
2025-06-09
Public Version Status
Update
Public Device Record Key
74641009-c6b3-440e-ac5e-f69fd17cdff3

Device Description

CranioFit PEEK Patient Specific Cranial/Craniofacial Implant(PSCI)

Device Characteristics

Single Use
Yes
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
MR Safe
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
GXN Plate, Cranioplasty, Preformed, Non-Alterable

GMDN Terms

Code Name
46268 Cranioplasty plate, non-alterable

Identifiers

Type ID
Primary M384CF260800160

Customer Contacts

Phone
888-246-7528