FDA UDI In Commercial Distribution 🇺🇸 United States

ROMEO ® 2 PAD INSTRUMENTATION

DI: 07640139349231 · Model: PAD-IN 01 00-N · SpineArt SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ROMEO ® 2 PAD INSTRUMENTATION
Primary DI
07640139349231
Version / Model
PAD-IN 01 00-N
Catalog Number
PAD-IN 01 00-N
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-31
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
0f977094-b23f-4b56-a66e-04138cf59668

Device Description

Process Preparer

Device Characteristics

Single Use
No
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
Yes
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
PEK Spinous Process Plate

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 07640139349231