FDA UDI In Commercial Distribution 🇺🇸 United States

OASYS Spinal System

DI: 07613327176285 · Model: 48850800 · Stryker Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OASYS Spinal System
Primary DI
07613327176285
Version / Model
48850800
Catalog Number
48850800
Company Name
Stryker Corporation
Labeler DUNS
149183167
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-01-18
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
9d2e234d-3a02-413c-823e-19d21ebb783a

Device Description

800-860 mm Transition Rod Tube

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
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 07613327176285