← Back to catalogue

Aesculap

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
Eustachian catheter, reusable FDA UDI
Device Name
HARTMANN Eustachian Catheter, diam. 3 mm FDA UDI
Model / Reference
OF252C FDA UDI
Description
HARTMANN Eustachian Catheter, diam. 3 mm FDA UDI

Identifiers

Catalog Number
OF252C FDA UDI
Primary DI / UDI-DI
04038653176267 FDA UDI
FDA Product Code
GBY FDA UDI
GMDN Term
Eustachian catheter, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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: Eustachian catheter, reusable

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

Similar devices

Also classified as Eustachian catheter, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI c7b8c460-7da2-4ad5-8814-835d7582faf9 35 fields · synced Jun 8, 2026