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Hyper LT

FDA UDI

Class U (US FDA UDI)

by Stryker Medtech K.k.

Identity

Trade Name
Hyper LT FDA UDI
Generic Name
Soft-tissue ultrasonic surgical system handpiece, reusable FDA UDI
Device Name
Angled Hard Tissue Curette Handpiece without Tip, 25 kHz FDA UDI
Model / Reference
5450814000 FDA UDI
Description
Angled Hard Tissue Curette Handpiece without Tip, 25 kHz FDA UDI

Identifiers

Catalog Number
5450-814-000 FDA UDI
Primary DI / UDI-DI
07613327289893 FDA UDI
FDA Product Code
LFL FDA UDI
GMDN Term
Soft-tissue ultrasonic surgical system handpiece, reusable FDA UDI

Classification

Device Class
U 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Soft-tissue ultrasonic surgical system handpiece, reusable

Hyper LT by Stryker Medtech K.k. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft-tissue ultrasonic surgical system handpiece, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Medtech K.k.

Sources (1)

  • FDA UDI 35e22887-23a1-4f2a-a55c-63377896eb1b 36 fields · synced Jun 6, 2026