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Aesculap

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
ENT trocar blade FDA UDI
Device Name
SINOSCOPY TROCAR AND CANNULA 5MM 165MM FDA UDI
Model / Reference
MA598R FDA UDI
Description
SINOSCOPY TROCAR AND CANNULA 5MM 165MM FDA UDI

Identifiers

Catalog Number
MA598R FDA UDI
Primary DI / UDI-DI
04046964588686 FDA UDI
FDA Product Code
KTE FDA UDI
GMDN Term
ENT trocar blade FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: ENT trocar blade

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

Similar devices

Also classified as ENT trocar blade.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 5c5d8abc-dd87-4627-8fdf-47a57c4fca67 35 fields · synced Jun 8, 2026