← Back to catalogue

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
Plug in the Spectra wearable adapter FDA UDI
Model / Reference
Spectra Wearable power adapter plug FDA UDI
Description
Plug in the Spectra wearable adapter FDA UDI

Identifiers

Catalog Number
MM55PRONGS FDA UDI
Primary DI / UDI-DI
08809108017918 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

Yes

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

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

Manufacturer

Sources (1)

  • FDA UDI 14158a70-d5d0-4bec-a0f4-16b884055c77 35 fields · synced May 30, 2026