AeroDR S33/S30

FDA UDI

Class II (US FDA UDI)

by Konica Minolta, Inc.

Identity

Trade Name: AeroDR S33/S30 FDA UDI
Generic Name: X-ray film cassette holder FDA UDI
Model / Reference: AACU FDA UDI

Identifiers

Primary DI / UDI-DI: 04560141946248 FDA UDI
510(k) Number: K121109 FDA UDI
FDA Product Code: KPR FDA UDI
GMDN Term: X-ray film cassette holder FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.1680 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: X-ray film cassette holder

AeroDR S33/S30 by Konica Minolta, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K121109 also covers:

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: Konica Minolta, Inc.

Sources (1)

FDA UDI 980bb6f3-c8a3-4d1c-8567-7fdf78fb10d9 33 fields · synced May 30, 2026