FDA UDI In Commercial Distribution 🇺🇸 United States

RHEAD

DI: 00886385023243 · Model: 313-0102 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RHEAD
Primary DI
00886385023243
Version / Model
313-0102
Catalog Number
313-0102
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2019-01-31
Public Version Status
Update
Public Device Record Key
9222b52f-2bb4-480b-9352-22e4307a93b8

Device Description

Std Ext. Stem Trial; 6mm Collar; Size 3

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
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
JDB PROSTHESIS, ELBOW, SEMI-CONSTRAINED, CEMENTED

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 00886385023243