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Aesculap

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
Tuning fork FDA UDI
Device Name
LUCAE TUNING FORK C2 512 FDA UDI
Model / Reference
OF017N FDA UDI
Description
LUCAE TUNING FORK C2 512 FDA UDI

Identifiers

Catalog Number
OF017N FDA UDI
Primary DI / UDI-DI
04038653013395 FDA UDI
FDA Product Code
GWX FDA UDI
GMDN Term
Tuning fork FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.1525 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Tuning fork

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

Similar devices

Also classified as Tuning fork.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 86d7d2f2-591f-4ea7-946b-6c9e323f0c0a 35 fields · synced Jun 7, 2026