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Aesculap

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
MINOP Micro Forceps, working length: 10 1/2", (265 mm), diam. 2 mm, rotatable, toothed (1x2), consisting of FF432R, FF433R, FF439R,detachable, to be used with: FF399R FDA UDI
Model / Reference
FF389R FDA UDI
Description
MINOP Micro Forceps, working length: 10 1/2", (265 mm), diam. 2 mm, rotatable, toothed (1x2), consisting of FF432R, FF433R, FF439R,detachable, to be used with: FF399R FDA UDI

Identifiers

Catalog Number
FF389R FDA UDI
Primary DI / UDI-DI
04038653163724 FDA UDI
FDA Product Code
GWG FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1480 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

No

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: Rigid endoscopic tissue manipulation forceps, reusable

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

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI c2a00dee-c66c-4e58-9217-182c8a84e834 36 fields · synced Jun 7, 2026