Identity
- Trade Name
- DR200 FDA UDI
- Generic Name
- Electrocardiographic long-term ambulatory recording analyser FDA UDI
- Device Name
- DR200 holter recorder w/ 7L patient cable FDA UDI
- Model / Reference
- DR200 7L FDA UDI
- Description
- DR200 holter recorder w/ 7L patient cable FDA UDI
Identifiers
- Catalog Number
- NEMK96 FDA UDI
- Primary DI / UDI-DI
- M581NEMK960 FDA UDI
- 510(k) Number
- K061293 FDA UDI
- FDA Product Code
- MWJ FDA UDI
- GMDN Term
- Electrocardiographic long-term ambulatory recording analyser FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2800 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
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 8.6 Centimeter FDA UDIWidth — 6.0 Centimeter FDA UDIDepth — 2.0 Centimeter FDA UDIWeight — 70.9 Gram FDA UDI
Category: Electrocardiographic long-term ambulatory recording analyser
Dr200 by North East Monitoring, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Electrocardiographic long-term ambulatory recording analyser.
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Cleared under the same submission
K061293 also covers:
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
- North East Monitoring, Inc.
Sources (1)
- FDA UDI 461cb9d9-d94b-43de-9fc1-b472864e4522 37 fields · synced May 29, 2026