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Guenter Bissinger Medizintechnik GmbH

FDA UDI

Class II (US FDA UDI)

by Günter Bissinger Medizintechnik GmbH

Identity

Trade Name
Guenter Bissinger Medizintechnik GmbH FDA UDI
Generic Name
Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI
Device Name
FROELICH Suction Tube 6 Fr., malleable, rotatable, WL 165 mm FDA UDI
Model / Reference
89817006 FDA UDI
Description
FROELICH Suction Tube 6 Fr., malleable, rotatable, WL 165 mm FDA UDI

Identifiers

Catalog Number
89817006 FDA UDI
Primary DI / UDI-DI
04250418753135 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Surgical irrigation/aspiration cannula, non-illuminating, reusable 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

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

Guenter Bissinger Medizintechnik GmbH by Günter Bissinger Medizintechnik GmbH — Class II — 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 05772576-5947-4c43-a7c1-81c3d64f0afd 35 fields · synced May 30, 2026