FDA UDI In Commercial Distribution 🇺🇸 United States

ClearFit

DI: 00855113008029 · Model: 171712 · LONGEVITI NEURO SOLUTIONS LLC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ClearFit
Primary DI
00855113008029
Version / Model
171712
Catalog Number
171712
Company Name
LONGEVITI NEURO SOLUTIONS LLC
Labeler DUNS
070659539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-21
Public Version
1
Public Version Date
2018-12-24
Public Version Status
New
Public Device Record Key
75dc6a7f-a85d-4bed-a3a0-abbf6c9fad98

Device Description

Large Static Cranial Implant (Primary and Backup)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GXN Plate, Cranioplasty, Preformed, Non-Alterable
PJN Filler, Bone Void, Non-Alterable Compound For Cranioplasty

GMDN Terms

Code Name
16131 Cranial resinous compound

Identifiers

Type ID
Primary 00855113008029
Package 10855113008026

Customer Contacts

Phone
410-527-1803

Premarket Submissions

Submission Number Supplement Number
K170410 000

Device Sizes

Type Value Unit Text
Area/Surface Area 60 Square centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
See special handling instructions
Type
Handling Environment Temperature
Temperature Range
59 – 86 Percent (%) Relative Humidity
Type
Storage Environment Humidity
Temperature Range
0 – 70 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
59 – 86 Degrees Fahrenheit