Identity
- Trade Name
- 5LD,PINCH TO DIN,UNSHIELDED,H,INTERMED FDA UDI
- Generic Name
- Electrocardiographic lead set, reusable FDA UDI
- Device Name
- 5LD,PINCH TO DIN,UNSHIELDED,H,INTERMED FDA UDI
- Model / Reference
- LW-3090040/5A-I FDA UDI
- Description
- 5LD,PINCH TO DIN,UNSHIELDED,H,INTERMED FDA UDI
Identifiers
- Catalog Number
- 18899 FDA UDI
- Primary DI / UDI-DI
- 00840828147323 FDA UDI
- FDA Product Code
- DSA FDA UDI
- GMDN Term
- Electrocardiographic lead set, reusable 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
5ld, Pinch To Din, Unshielded, H, 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 87e76c31-cf3d-4ca2-ad86-a2bfe198ac96 36 fields · synced May 31, 2026