← Back to catalogue

AeroTech I Shield

FDA UDI

Class II (US FDA UDI)

by Mirion Technologies (capintec), Inc

Identity

Trade Name
AeroTech I Shield FDA UDI
Generic Name
Radioaerosol administration set FDA UDI
Device Name
AeroTech I Shield, part of Radioaerosol Administration System FDA UDI
Model / Reference
177-095 FDA UDI
Description
AeroTech I Shield, part of Radioaerosol Administration System FDA UDI

Identifiers

Catalog Number
177-095 FDA UDI
Primary DI / UDI-DI
00879942070101 FDA UDI
510(k) Number
K800023 FDA UDI
FDA Product Code
IYT FDA UDI
GMDN Term
Radioaerosol administration set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1390 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

Yes

FDA UDI

Category: Radioaerosol administration set

AeroTech I Shield by Mirion Technologies (capintec), Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radioaerosol administration set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 280d2ea5-02f6-4556-b176-dabc7a516fbf 36 fields · synced Jun 8, 2026