FDA UDI In Commercial Distribution 🇺🇸 United States

ROMEO 2 INSTRUMENTATION

DI: 07640151084271 · Model: MIS-IN 06 06-N · SpineArt SA
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ROMEO 2 INSTRUMENTATION
Primary DI
07640151084271
Version / Model
MIS-IN 06 06-N
Catalog Number
MIS-IN 06 06-N
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-19
Public Version
1
Public Version Date
2019-01-21
Public Version Status
New
Public Device Record Key
7fcc101e-e7bd-4f99-a7a0-2d253b101616

Device Description

DILATOR TUBE 4 PUSHER

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
KWP Appliance, Fixation, Spinal Interlaminal
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

Code Name
47829 Surgical instrument handle, non-torque-limiting

Identifiers

Type ID
Primary 07640151084271