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SCANLAN® Minimally Invasive Instrumentation

FDA UDI

Class II (US FDA UDI)

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Minimally Invasive Instrumentation FDA UDI
Generic Name
General-purpose surgical suction system, vacuum FDA UDI
Device Name
SCANLAN® Dennis Suction Instrument Knurled Blunt Tip FDA UDI
Model / Reference
9009-916K FDA UDI
Description
SCANLAN® Dennis Suction Instrument Knurled Blunt Tip FDA UDI

Identifiers

Catalog Number
9009-916K FDA UDI
Primary DI / UDI-DI
00846159014532 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
General-purpose surgical suction system, vacuum FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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: General-purpose surgical suction system, vacuum

SCANLAN® Minimally Invasive Instrumentation by Scanlan International Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose surgical suction system, vacuum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Scanlan International Inc

Sources (1)

  • FDA UDI 20895ef6-b9e2-4173-a3d2-66e6dcfff07b 35 fields · synced May 30, 2026