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Spectra

FDA UDI

Class II (US FDA UDI)

by Uzinmedicare Co., Ltd.

Identity

Trade Name
Spectra FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Power adapter for Spectra wearable FDA UDI
Model / Reference
Spectra Wearable power adapter FDA UDI
Description
Power adapter for Spectra wearable FDA UDI

Identifiers

Catalog Number
MM550002-S FDA UDI
Primary DI / UDI-DI
08809108017901 FDA UDI
510(k) Number
K220926 FDA UDI
FDA Product Code
HGX FDA UDI
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5160 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

Yes

FDA UDI

Category: Electrical-only medical device connection cable, reusable

Spectra by Uzinmedicare Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 824f09ac-9ba1-4848-9ab3-02dc002cb4f6 35 fields · synced May 30, 2026