FDA UDI In Commercial Distribution 🇺🇸 United States

Epiphany

DI: B528PSE5522140 · Model: 1 · PANTHEON SPINAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Epiphany
Primary DI
B528PSE5522140
Version / Model
1
Catalog Number
PSE 55-22-14
Company Name
PANTHEON SPINAL, LLC
Labeler DUNS
071012634
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-21
Public Version
1
Public Version Date
2020-04-29
Public Version Status
New
Public Device Record Key
9349fb4e-0748-4a40-9410-889884399e4a

Device Description

Epiphany RLIF Cage 55x22x14mm

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
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
No
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary B528PSE5522140

Customer Contacts

Phone
5122154888

Device Sizes

Type Value Unit Text
Height 14 Millimeter
Length 55 Millimeter
Width 22 Millimeter