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Eikon LT Adapt Smoke Evacuation

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Eikon LT Adapt Smoke Evacuation FDA UDI
Generic Name
Fibreoptic retractor handle FDA UDI
Device Name
LT Adapt Smoke Evacuation Retractor, 155mm, Reusable Slat FDA UDI
Model / Reference
S155 FDA UDI
Description
LT Adapt Smoke Evacuation Retractor, 155mm, Reusable Slat FDA UDI

Identifiers

Catalog Number
S155 FDA UDI
Primary DI / UDI-DI
30816728021552 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Fibreoptic retractor handle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Dimensions & Sizes

Size
Length — 155 Millimeter FDA UDI

Category: Fibreoptic retractor handle

Eikon LT Adapt Smoke Evacuation by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic retractor handle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 0b88de00-57b8-4bbc-8ff0-12a30afc654e 36 fields · synced May 30, 2026