← Back to catalogue

MUSE Staple Cartridge

FDA UDI

Class II (US FDA UDI)

by Medigus , Ltd.

Identity

Trade Name
MUSE Staple Cartridge FDA UDI
Generic Name
Surgical staple loading unit, non-cutting FDA UDI
Device Name
Each box contains 30 sterile single use cartridges Each cartridge contains five standard 4.8 mm titanium staples FDA UDI
Model / Reference
02 FDA UDI
Description
Each box contains 30 sterile single use cartridges Each cartridge contains five standard 4.8 mm titanium staples FDA UDI

Identifiers

Catalog Number
MMAA9001011 FDA UDI
Primary DI / UDI-DI
07290014036079 FDA UDI
FDA Product Code
ODE FDA UDI
GMDN Term
Surgical staple loading unit, non-cutting 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical staple loading unit, non-cutting

MUSE Staple Cartridge by Medigus , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical staple loading unit, non-cutting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medigus , Ltd.

Sources (1)

  • FDA UDI 69d03cff-a294-4b00-bf36-e314f7f6ac86 35 fields · synced May 30, 2026