FDA UDI In Commercial Distribution 🇺🇸 United States

PERPOS FCD-2 System

DI: 81195401011900 · Model: 9061-00 · INTERVENTIONAL SPINE, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PERPOS FCD-2 System
Primary DI
81195401011900
Version / Model
9061-00
Catalog Number
9061-00
Company Name
INTERVENTIONAL SPINE, INC
Labeler DUNS
017663522
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-15
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
219f6eab-f305-4f51-bfa6-dc9da17f4a84

Device Description

Instruments with Teleport and Tray

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 81195401011900

Customer Contacts

Phone
800-497-0484