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Aesculap

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
Rigid optical intracranial/spinal endoscope, reusable FDA UDI
Device Name
PAEDISCOPE EYEPIECE FDA UDI
Model / Reference
PF011A FDA UDI
Description
PAEDISCOPE EYEPIECE FDA UDI

Identifiers

Catalog Number
PF011A FDA UDI
Primary DI / UDI-DI
04038653320554 FDA UDI
FDA Product Code
GWG FDA UDI
GMDN Term
Rigid optical intracranial/spinal endoscope, 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid optical intracranial/spinal endoscope, reusable

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

Similar devices

Also classified as Rigid optical intracranial/spinal endoscope, 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 dd19f0b0-eaa0-4294-839f-40f7c575fbad 35 fields · synced May 30, 2026