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Morce Power Plus

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
MORCE POWER PLUS FDA UDI
Generic Name
Laparoscopic access cannula, reusable FDA UDI
Device Name
PROTECTION SLEEVE CAP 12MM WL 184MM stainless steel-sheath tube smooth, with distal tissue positioner, reusable FDA UDI
Model / Reference
83070128 FDA UDI
Description
PROTECTION SLEEVE CAP 12MM WL 184MM stainless steel-sheath tube smooth, with distal tissue positioner, reusable FDA UDI

Identifiers

Catalog Number
83070128 FDA UDI
Primary DI / UDI-DI
04055207007648 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Laparoscopic access cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

No

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

Dimensions & Sizes

Size
Length — 184 Millimeter FDA UDI

Category: Laparoscopic access cannula, reusable

Morce Power Plus by Richard Wolf GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic access cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI 1a0160fa-3a40-4249-a153-78740de59726 36 fields · synced May 30, 2026