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W&H

FDA UDI

Class II (US FDA UDI)

by Miele & Cie. KG

Identity

Trade Name
W&H FDA UDI
Generic Name
Surgical instrument washer/disinfector (chemical/thermal) FDA UDI
Device Name
washer disinfector FDA UDI
Model / Reference
Teon+ RID-200 FDA UDI
Description
washer disinfector FDA UDI

Identifiers

Primary DI / UDI-DI
04002516174103 FDA UDI
FDA Product Code
MEC FDA UDI
GMDN Term
Surgical instrument washer/disinfector (chemical/thermal) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6992 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

W&H by Miele & Cie. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Miele & Cie. KG

Sources (1)

  • FDA UDI 657ea2a6-382f-4687-b932-fc3e688a87c1 34 fields · synced Jun 8, 2026