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CardioFIT

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
CardioFIT FDA UDI
Generic Name
Rigid endoscopic grasping forceps, reusable FDA UDI
Device Name
CardioFIT Forceps Insert FDA UDI
Model / Reference
49310CMH FDA UDI
Description
CardioFIT Forceps Insert FDA UDI

Identifiers

Primary DI / UDI-DI
04048551404690 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Rigid endoscopic grasping forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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: Rigid endoscopic grasping forceps, reusable

CardioFIT by Karl Storz GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic grasping forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Karl Storz GmbH & Co. KG

Sources (1)

  • FDA UDI dfe8e837-e5f2-4b0c-b46a-d27def7111d1 33 fields · synced Jun 8, 2026