LITe

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: LITe FDA UDI
Generic Name: Nerve-locating system probe, single-use FDA UDI
Device Name: Y-Needle 200 FDA UDI
Model / Reference: DI_48850200 FDA UDI
Description: Y-Needle 200 FDA UDI

Identifiers

Catalog Number: 48850200 FDA UDI
Primary DI / UDI-DI: 07613327359619 FDA UDI
510(k) Number: K171807 FDA UDI
FDA Product Code: PDQ FDA UDI
GMDN Term: Nerve-locating system probe, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 874.1820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nerve-locating system probe, single-use

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

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Also classified as Nerve-locating system probe, single-use.

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Cleared under the same submission

K171807 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI 9afa6db3-8821-4c97-9936-eb0e8cb24fea 35 fields · synced May 30, 2026