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Dr 1817

FDA UDI

Class I (US FDA UDI)

by Philips Medical Systems GmbH, Dmc

Identity

Trade Name
DR 1817 FDA UDI
Generic Name
X-ray tube housing assembly, diagnostic FDA UDI
Device Name
diagnostic x-ray tube housing assembly FDA UDI
Model / Reference
9890-000-86151 FDA UDI
Description
diagnostic x-ray tube housing assembly FDA UDI

Identifiers

Catalog Number
9890-000-86151 FDA UDI
Primary DI / UDI-DI
00884838076372 FDA UDI
FDA Product Code
ITY FDA UDI
GMDN Term
X-ray tube housing assembly, diagnostic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1760 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: X-ray tube housing assembly, diagnostic

Dr 1817 by Philips Medical Systems GmbH, Dmc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray tube housing assembly, diagnostic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 882ab155-fa8c-4f32-80e9-4ba5f7bd7811 34 fields · synced Jun 6, 2026