FDA UDI Not in Commercial Distribution 🇺🇸 United States

PERPOS PLS SYSTEM

DI: 81195401062186 · Model: 9045-00 · INTERVENTIONAL SPINE, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PERPOS PLS SYSTEM
Primary DI
81195401062186
Version / Model
9045-00
Catalog Number
9045-00
Company Name
INTERVENTIONAL SPINE, INC
Labeler DUNS
017663522
Distribution Status
Not 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
2dffedeb-8c0a-4366-ab2a-bb67c36bc953
Distribution End Date
2016-12-23

Device Description

Perpos PLS System, Instrument Kit Only

Device Characteristics

Single Use
Yes
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
MR Safe
Direct Marking Exempt
No
PM Exempt
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44052 Orthopaedic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 81195401062186

Customer Contacts

Phone
800-497-0484