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AeroDR Stitching Barrier Unit

FDA UDI

Class II (US FDA UDI)

by Konica Minolta, Inc.

Identity

Trade Name
AeroDR Stitching Barrier Unit FDA UDI
Generic Name
Radiation shielding panel, portable/mobile FDA UDI
Model / Reference
A5EX FDA UDI

Identifiers

Primary DI / UDI-DI
04560141936768 FDA UDI
510(k) Number
K120752 FDA UDI
FDA Product Code
KPR FDA UDI
GMDN Term
Radiation shielding panel, portable/mobile 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Radiation shielding panel, portable/mobile

AeroDR Stitching Barrier Unit by Konica Minolta, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation shielding panel, portable/mobile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 718cac70-e5bc-41a1-8af6-a9314f02e44f 33 fields · synced Jun 8, 2026