FDA UDI In Commercial Distribution 🇺🇸 United States

ROCCIA

DI: 04054896019796 · Model: S-RPP-09112805-S · Silony Medical GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ROCCIA
Primary DI
04054896019796
Version / Model
S-RPP-09112805-S
Catalog Number
S-RPP-09112805-S
Company Name
Silony Medical GmbH
Labeler DUNS
312969760
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-15
Public Version
2
Public Version Date
2023-08-29
Public Version Status
Update
Public Device Record Key
fa29aded-10c7-4c20-90fb-0e111db26c33

Device Description

ROCCIA PLIF Cage, 9x11x28mm, 5° lor.

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary 04054896019796

Device Sizes

Type Value Unit Text
Length 28 Millimeter
Angle 5 degree
Height 9 Millimeter
Width 11 Millimeter