FDA UDI In Commercial Distribution 🇺🇸 United States

OmniPore Surgical Implant

DI: 00855421005963 · Model: OP7511 · MATRIX SURGICAL HOLDINGS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OmniPore Surgical Implant
Primary DI
00855421005963
Version / Model
OP7511
Company Name
MATRIX SURGICAL HOLDINGS, LLC
Labeler DUNS
079634199
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-20
Public Version
1
Public Version Date
2020-04-28
Public Version Status
New
Public Device Record Key
092b2427-31ad-4cb7-af2c-cdf3fdf5536d

Device Description

Burr Hole Cover

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
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
KKY Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

GMDN Terms

Code Name
33310 Polyethylene craniofacial tissue reconstructive material

Identifiers

Type ID
Primary 00855421005963

Premarket Submissions

Submission Number Supplement Number
K123908 000