Identity
- Trade Name
- Easy@Home Fingertip Pulse Oximeter FDA UDI
- Generic Name
- Telemetric pulse oximeter FDA UDI
- Model / Reference
- EHP50D1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850253007116 FDA UDI
- 510(k) Number
- K082641 FDA UDI
- FDA Product Code
- OCH FDA UDI
- GMDN Term
- Telemetric pulse oximeter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2700 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Telemetric pulse oximeter
Easy@Home Fingertip Pulse Oximeter by Easy Healthcare Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K082641 also covers:
- Care One — Ahold U.S.A., Inc.
- Amazon Basic Care — Amazon.com Services, LLC
- Good Neighbor — Amerisourcebergen Drug Corporation
- Good Neighbor — Amerisourcebergen Drug Corporation
- Pulse oximeter — BETTER BASICS, INC.
- Curaplex — BOUND TREE MEDICAL, LLC
- QUALITY CHOICE — CHAIN DRUG MARKETING ASSOCIATION, INC.
- microdot® — Cambridge Sensors USA, LLC.
- LEADER — Cardinal Health 110, Inc.
- LEADER — Cardinal Health 110, Inc.
- Virginia National Guard — Clinical Guard
- CONTEC — Contec Medical Systems 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 |
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Manufacturer
- Manufacturer
- Easy Healthcare Corporation
Sources (1)
- FDA UDI 3eeab0d5-7117-406c-985f-1c863889da82 33 fields · synced May 30, 2026