Identity
- Trade Name
- DLW,3LD,PINCH,INTELVUE,"XX",AHA,INTERMED FDA UDI
- Generic Name
- Electrocardiographic electrode, single-use FDA UDI
- Device Name
- DLW,3LD,PINCH,INTELVUE,"XX",AHA,INTERMED FDA UDI
- Model / Reference
- DLW-03BK-40AS-3000 FDA UDI
- Description
- DLW,3LD,PINCH,INTELVUE,"XX",AHA,INTERMED FDA UDI
Identifiers
- Catalog Number
- 18930 FDA UDI
- Primary DI / UDI-DI
- 90840828100840 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
Dlw, 3ld, Pinch, Intelvue, "xx", Aha, 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 |
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Manufacturer
- Manufacturer
- Curbell Medical Products, Inc.
Sources (1)
- FDA UDI b4f3f221-12de-4eae-aaf4-3af4f35f753f 36 fields · synced Jun 8, 2026