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Aesculap

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
Laparoscopic dilation guide rod FDA UDI
Device Name
TROCAR PIN TRIANGULAR 12/150MM FDA UDI
Model / Reference
EK073R FDA UDI
Description
TROCAR PIN TRIANGULAR 12/150MM FDA UDI

Identifiers

Catalog Number
EK073R FDA UDI
Primary DI / UDI-DI
04046963425241 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic dilation guide rod FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

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: Laparoscopic dilation guide rod

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

Similar devices

Also classified as Laparoscopic dilation guide rod.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI e00cc21b-3a31-43d5-bbb0-a9652b8d8d85 36 fields · synced Jun 1, 2026