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SCANLAN® Dissector

FDA UDI

Class I (US FDA UDI)

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Dissector FDA UDI
Generic Name
ENT elevator FDA UDI
Device Name
Freer Style Elevator FDA UDI
Model / Reference
4004-118U FDA UDI
Description
Freer Style Elevator FDA UDI

Identifiers

Catalog Number
4004-118U FDA UDI
Primary DI / UDI-DI
00846159035667 FDA UDI
FDA Product Code
GZX FDA UDI
GMDN Term
ENT elevator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4525 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: ENT elevator

SCANLAN® Dissector by Scanlan International Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT elevator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 53585035-c6b1-4673-90c5-41fbb9a373cd 35 fields · synced May 30, 2026