Aesculap

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name: AESCULAP FDA UDI
Generic Name: Neurosurgical microscope FDA UDI
Device Name: AESCULAP AEOS FDA UDI
Model / Reference: PV010 FDA UDI
Description: AESCULAP AEOS FDA UDI

Identifiers

Catalog Number: PV010 FDA UDI
Primary DI / UDI-DI: 04046955206742 FDA UDI
FDA Product Code: FSO FDA UDI
GMDN Term: Neurosurgical microscope FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4700 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Neurosurgical microscope

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

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Also classified as Neurosurgical microscope.

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OPMI® PENTERO® 900 — Carl Zeiss Meditec AG · Class I
BLUE 400 — Carl Zeiss Meditec AG · Class I
RE3 — DIGITAL SURGERY SYSTEMS, INC · Class I
Surgical Microscope MM80/YOH — MITAKA KOHKI CO., LTD. · Class I
Surgical Microscope MM80/SS1 — MITAKA KOHKI CO., LTD. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Aesculap, Inc.

Sources (1)

FDA UDI fad88e76-174b-4ec8-873d-3acda9d61952 35 fields · synced May 30, 2026