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MIP Minimal Invasive PCNL

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
MIP Minimal Invasive PCNL FDA UDI
Generic Name
Flexible endoscopic biopsy forceps, reusable FDA UDI
Device Name
Biopsy Forceps, 5 Fr. FDA UDI
Model / Reference
27830FL FDA UDI
Description
Biopsy Forceps, 5 Fr. FDA UDI

Identifiers

Catalog Number
27830FL FDA UDI
Primary DI / UDI-DI
04048551090619 FDA UDI
FDA Product Code
OCZ FDA UDI
GMDN Term
Flexible endoscopic biopsy forceps, reusable 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

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: Flexible endoscopic biopsy forceps, reusable

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

Similar devices

Also classified as Flexible endoscopic biopsy 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 a63ab53a-6744-42df-a14c-1533dc40638d 35 fields · synced May 31, 2026