FDA UDI In Commercial Distribution 🇺🇸 United States

ARIA

DI: 07613327272178 · Model: 48758218 · Stryker Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ARIA
Primary DI
07613327272178
Version / Model
48758218
Catalog Number
48758218
Company Name
Stryker Corporation
Labeler DUNS
149183167
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-20
Public Version
1
Public Version Date
2019-11-28
Public Version Status
New
Public Device Record Key
9b34bf33-2b22-4db2-807b-6aeb6ac0dd60

Device Description

REAMER DISTRACTOR

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
56637 Orthopaedic surgical distractor, internal

Identifiers

Type ID
Primary 07613327272178

Device Sizes

Type Value Unit Text
Height 18.0 Millimeter
Length 60.0 Millimeter