Identity
- Trade Name
- 100mm x 22m ECG Printer Paper (2/roll) FDA UDI
- Generic Name
- Patient monitoring system module, printing FDA UDI
- Device Name
- PAPER ROLLS, 100MM WIDE,ECG FDA UDI
- Model / Reference
- 11240 FDA UDI
- Description
- PAPER ROLLS, 100MM WIDE,ECG FDA UDI
Identifiers
- Catalog Number
- 11240-000016 FDA UDI
- Primary DI / UDI-DI
- 00681490597722 FDA UDI
- FDA Product Code
- DSF FDA UDI
- GMDN Term
- Patient monitoring system module, printing FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.2810 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
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
100mm x 22m ECG Printer Paper (2/roll) by PHYSIO-CONTROL, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- PHYSIO-CONTROL, Inc.
Sources (1)
- FDA UDI ead7f982-e9af-49b9-96fe-3a5599330a1b 36 fields · synced Jun 9, 2026