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Minop

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
MINOP FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
MINOP Suction Cannula, 45 °, straight, diam. 2 mm, sharp, sterile, disposable, to be used with: FF399R FDA UDI
Model / Reference
FH607SU FDA UDI
Description
MINOP Suction Cannula, 45 °, straight, diam. 2 mm, sharp, sterile, disposable, to be used with: FF399R FDA UDI

Identifiers

Catalog Number
FH607SU FDA UDI
Primary DI / UDI-DI
04046963442811 FDA UDI
FDA Product Code
GCY FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4680 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical irrigation/aspiration tubing set

Minop by Aesculap, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 801a42ab-e179-4ce2-bf6a-de17fed4396a 35 fields · synced May 31, 2026