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Cannula, Suction, acc. Bugge 29cm Ø10mm medium

FDA UDI

Class I (US FDA UDI)

by Geister Medizin Technik GmbH

Identity

Trade Name
Cannula, Suction, acc. Bugge 29cm Ø10mm medium FDA UDI
Generic Name
Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI
Device Name
Cannula, Suction, acc. Bugge 29cm Ø10mm medium FDA UDI
Model / Reference
18-0402 FDA UDI
Description
Cannula, Suction, acc. Bugge 29cm Ø10mm medium FDA UDI

Identifiers

Catalog Number
18-0402 FDA UDI
Primary DI / UDI-DI
04057034040232 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Surgical irrigation/aspiration cannula, non-illuminating, reusable 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

No

FDA UDI

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

Cannula, Suction, acc. Bugge 29cm Ø10mm medium by Geister Medizin Technik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 739d0a9f-5d0f-4bc7-bc41-8a0c60501665 35 fields · synced May 31, 2026