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Karl Schumacher

FDA UDI

Class I (US FDA UDI)

by Karl Schumacher Dental, Llc

Identity

Trade Name
Karl Schumacher FDA UDI
Generic Name
Dental suction system cannula, reusable FDA UDI
Device Name
6x4mm BackCut Asp w/Relief Slot #46FSABC FDA UDI
Model / Reference
ASP0046FSABC FDA UDI
Description
6x4mm BackCut Asp w/Relief Slot #46FSABC FDA UDI

Identifiers

Primary DI / UDI-DI
00842517104846 FDA UDI
FDA Product Code
EHZ FDA UDI
GMDN Term
Dental suction system cannula, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

No

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: Dental suction system cannula, reusable

Karl Schumacher by Karl Schumacher Dental, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental suction system cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8c12cffe-661e-4800-94a2-3f4c5089f9ae 34 fields · synced Jun 1, 2026