FDA UDI Not in Commercial Distribution 🇺🇸 United States

RHEAD

DI: 00886385023359 · Model: 603-0100 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RHEAD
Primary DI
00886385023359
Version / Model
603-0100
Catalog Number
603-0100
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
10
Public Version Date
2023-08-18
Public Version Status
Update
Public Device Record Key
5af56a59-f1a6-4e35-9576-d311ae302e6b
Distribution End Date
2023-08-17

Device Description

Extended Stem; Instrument Tray; Base

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
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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 00886385023359