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
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Also classified as Electrical-only medical device connection cable, reusable.
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- Connection Cable — Shenzhen Keborui Electronics Co., Ltd · Class I
- TC-HEART LUNG DIN INTFC CA STOCKET — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
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Cleared under the same submission
K220926 also covers:
- Spectra — Uzinmedicare Co., Ltd.
- Spectra — Uzinmedicare Co., Ltd.
- Spectra — Uzinmedicare Co., Ltd.
- Spectra — Uzinmedicare Co., Ltd.
- Spectra — Uzinmedicare Co., Ltd.
- Spectra — Uzinmedicare Co., Ltd.
- Spectra — Uzinmedicare Co., Ltd.
- Spectra — Uzinmedicare Co., Ltd.
- Spectra — Uzinmedicare Co., Ltd.
- Spectra — Uzinmedicare Co., Ltd.
- Spectra — Uzinmedicare Co., Ltd.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Uzinmedicare Co., Ltd.
Sources (1)
- FDA UDI 14158a70-d5d0-4bec-a0f4-16b884055c77 35 fields · synced May 30, 2026