Identity
- Trade Name
- DISP ECG LW,5LD,PINCH TO MULTI,INTERMED FDA UDI
- Generic Name
- Electrocardiographic electrode, single-use FDA UDI
- Device Name
- DISP ECG LW,5LD,PINCH TO MULTI,INTERMED FDA UDI
- Model / Reference
- DLW-05BM-40AM-3000 FDA UDI
- Description
- DISP ECG LW,5LD,PINCH TO MULTI,INTERMED FDA UDI
Identifiers
- Catalog Number
- 18601 FDA UDI
- Primary DI / UDI-DI
- 90840828101014 FDA UDI
- FDA Product Code
- DSA FDA UDI
- GMDN Term
- Electrocardiographic electrode, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2900 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Disp Ecg Lw, 5ld, Pinch To Multi, Intermed by Curbell Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Curbell Medical Products, Inc.
Sources (1)
- FDA UDI 0e0b95c8-632c-4b9c-b740-4161d8277c3e 36 fields · synced May 31, 2026