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Eicken antrum cannula

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 30-101-30

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name
Eicken antrum cannula FDA UDI
Generic Name
Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI
Device Name
Suction and Irrigation Instruments EUDAMED
long curve, Ø 3.0 mm FDA UDI
Model / Reference
30-101-30 EUDAMEDFDA UDI
Description
long curve, Ø 3.0 mm FDA UDI

Identifiers

Catalog Number
30-101-30 FDA UDI
Primary DI / UDI-DI
04250381812334 EUDAMEDFDA UDI
Basic UDI-DI
B-04250381812334 EUDAMED
FDA Product Code
KAM FDA UDI
EMDN Code
L030101 SUCTION AND IRRIGATION SURGICAL CANNULAS AND HANDPIECES, REUSABLE EUDAMED
GMDN Term
Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Category: Surgical irrigation/aspiration cannula, non-illuminating, reusable

Eicken antrum cannula by Spiggle & Theis Medizintechnik GmbH — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration cannula, non-illuminating, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 638fbae9-6195-4fab-9cbb-e09e72f98ca0 35 fields · synced Oct 9, 2026
  • EUDAMED fe252570-f240-4606-97e2-de5918d4ceef 61 fields · synced Oct 9, 2026