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Reflex Hybrid

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
REFLEX HYBRID FDA UDI
Generic Name
Orthopaedic implant driver FDA UDI
Device Name
REVISION DRIVER FDA UDI
Model / Reference
48511906 FDA UDI
Description
REVISION DRIVER FDA UDI

Identifiers

Catalog Number
48511906 FDA UDI
Primary DI / UDI-DI
07613327271003 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic implant driver FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implant driver

Reflex Hybrid by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant driver.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI dce1fd55-9c35-415c-acc2-7110ce7aced2 34 fields · synced May 30, 2026