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Rhead

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
RHEAD FDA UDI
Generic Name
Uncoated elbow humerus prosthesis FDA UDI
Device Name
Standard Extended Stem, 6mm Collar, Size 4 FDA UDI
Model / Reference
410-0103 FDA UDI
Description
Standard Extended Stem, 6mm Collar, Size 4 FDA UDI

Identifiers

Catalog Number
410-0103 FDA UDI
Primary DI / UDI-DI
00886385023335 FDA UDI
FDA Product Code
JDB FDA UDI
GMDN Term
Uncoated elbow humerus prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3160 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Uncoated elbow humerus prosthesis

Rhead by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated elbow humerus prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI ec181d16-b4b9-4229-8a63-d149786e37b3 34 fields · synced Jun 8, 2026