FDA UDI In Commercial Distribution 🇺🇸 United States

SU-POR Surgical Implant

DI: 00815285020137 · Model: 4013 · PORIFEROUS, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SU-POR Surgical Implant
Primary DI
00815285020137
Version / Model
4013
Catalog Number
4013
Company Name
PORIFEROUS, LLC
Labeler DUNS
078388975
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-23
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
ae3ae38d-a885-42c5-94d4-90fd0ea9c591

Device Description

Sheet 50mm x 76mm x 1.5mm

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FWP Prosthesis, Chin, Internal
KKY Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

GMDN Terms

Code Name
33310 Polyethylene craniofacial tissue reconstructive material

Identifiers

Type ID
Primary 00815285020137

Customer Contacts

Phone
7706833855

Premarket Submissions

Submission Number Supplement Number
K140437 000