Identity
- Trade Name
- BIA Subject Cables FDA UDI
- Generic Name
- Analytical non-scalp cutaneous lead FDA UDI
- Device Name
- LEMO Subject Cables (6 ft / 1.8 m Length) FDA UDI
- Model / Reference
- LEMO Subject Cables (6 ft) FDA UDI
- Description
- LEMO Subject Cables (6 ft / 1.8 m Length) FDA UDI
Identifiers
- Catalog Number
- SCLEM6 FDA UDI
- Primary DI / UDI-DI
- B202SCLEM60 FDA UDI
- FDA Product Code
- IKD FDA UDI
- GMDN Term
- Analytical non-scalp cutaneous lead 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
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Analytical non-scalp cutaneous lead
BIA Subject Cables by R.j.l. Sciences, 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
- R.j.l. Sciences, Inc.
Sources (1)
- FDA UDI ff108f56-9eb1-4211-9d15-21ce654b6d6d 35 fields · synced May 30, 2026