Identity
- Trade Name
- Map-iT FDA UDI
- Generic Name
- Electrocardiographic lead/catheter adaptor FDA UDI
- Device Name
- Mapping Catheter Extension Cable: deca fixed, duo-deca fixed, duo-deca steerable, 14-pin female FDA UDI
- Model / Reference
- 901959 FDA UDI
- Description
- Mapping Catheter Extension Cable: deca fixed, duo-deca fixed, duo-deca steerable, 14-pin female FDA UDI
Identifiers
- Catalog Number
- 901959 FDA UDI
- Primary DI / UDI-DI
- 00818083019921 FDA UDI
- FDA Product Code
- IKD FDA UDI
- GMDN Term
- Electrocardiographic lead/catheter adaptor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.1175 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 210 Centimeter FDA UDI
Category: Electrocardiographic lead/catheter adaptor
Map-iT by Access Point Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Access Point Technologies, Inc.
Sources (1)
- FDA UDI 9bff6edb-18fd-45c7-a0ae-d47e515ebbd1 35 fields · synced May 30, 2026