Foot Switch Drapes

FDA UDI

Class II (US FDA UDI)

by Carl Zeiss Meditec AG

Identity

Trade Name: Foot Switch Drapes FDA UDI
Generic Name: Medical equipment/instrument drape, reusable FDA UDI
Model / Reference: 326012-0000-000 FDA UDI

Identifiers

Primary DI / UDI-DI: 04049539101952 FDA UDI
FDA Product Code: KKX FDA UDI
GMDN Term: Medical equipment/instrument drape, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4370 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Height — 24 Inch FDA UDI
Width — 14 Inch FDA UDI
Height — 61 Centimeter FDA UDI
Width — 36 Centimeter FDA UDI

Category: Medical equipment/instrument drape, reusable

Foot Switch Drapes by Carl Zeiss Meditec AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Carl Zeiss Meditec AG

Sources (1)

FDA UDI a7dea1d8-1d79-4a9f-816f-ad0007082366 33 fields · synced Jun 8, 2026