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Sierra Wave

FDA UDI

Class II (US FDA UDI)

by Cadwell Industries, Inc.

Identity

Trade Name
Sierra Wave FDA UDI
Generic Name
Electromyograph FDA UDI
Device Name
Skin Temperature Probe FDA UDI
Model / Reference
199210-200 FDA UDI
Description
Skin Temperature Probe FDA UDI

Identifiers

Primary DI / UDI-DI
00840067102046 FDA UDI
FDA Product Code
GWF FDA UDI
GWE FDA UDI
GWQ FDA UDI
IKN FDA UDI
OLT FDA UDI
JXE FDA UDI
GWJ FDA UDI
OLV FDA UDI
GMDN Term
Electromyograph FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1870 FDA UDI
882.1890 FDA UDI
882.1400 FDA UDI
890.1375 FDA UDI
882.1550 FDA UDI
882.1900 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electromyograph

Sierra Wave by Cadwell Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromyograph.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cadwell Industries, Inc.

Sources (1)

  • FDA UDI 8d2f5ced-f4bb-4894-a56c-19c9af8be480 34 fields · synced Jun 9, 2026