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Aesculap

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
Aneurysm clip applier FDA UDI
Device Name
YASARGIL Clip Applier Forceps, 7", (180 mm), with ratchet, mini, phynox, non-sterile, reusable FDA UDI
Model / Reference
FE548K FDA UDI
Description
YASARGIL Clip Applier Forceps, 7", (180 mm), with ratchet, mini, phynox, non-sterile, reusable FDA UDI

Identifiers

Catalog Number
FE548K FDA UDI
Primary DI / UDI-DI
04038653161447 FDA UDI
FDA Product Code
HCI FDA UDI
GMDN Term
Aneurysm clip applier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4175 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: Aneurysm clip applier

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

Similar devices

Also classified as Aneurysm clip applier.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 9801984a-14e7-4d1d-8973-f61ce974658c 35 fields · synced Jun 7, 2026