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EUROPCLIP Applier

FDA UDI

Class I (US FDA UDI)

by Ackermann Instrumente GmbH

Identity

Trade Name
EUROPCLIP Applier FDA UDI
Generic Name
Endoscopic surgical ligation clip applier, reusable FDA UDI
Device Name
Clip Applicator for Large Clips, Rotable, Double Action, 330 mm, Ø12,5 mm FDA UDI
Model / Reference
13-1613-106AS FDA UDI
Description
Clip Applicator for Large Clips, Rotable, Double Action, 330 mm, Ø12,5 mm FDA UDI

Identifiers

Primary DI / UDI-DI
04250302286008 FDA UDI
FDA Product Code
HBT FDA UDI
GMDN Term
Endoscopic surgical ligation clip applier, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscopic surgical ligation clip applier, reusable

EUROPCLIP Applier by Ackermann Instrumente GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic surgical ligation clip applier, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ackermann Instrumente GmbH

Sources (1)

  • FDA UDI 9b59b271-2efb-4dda-b936-18ca0ae7dd43 34 fields · synced May 30, 2026