Identity
- Trade Name
- Vermed FDA UDI
- Generic Name
- Electrocardiographic recording paper FDA UDI
- Device Name
- Electrocardiographic recording paper FDA UDI
- Model / Reference
- LTN 781-080-12 FDA UDI
- Description
- Electrocardiographic recording paper FDA UDI
Identifiers
- Catalog Number
- 01082320 FDA UDI
- Primary DI / UDI-DI
- 00009336000647 FDA UDI
- FDA Product Code
- DSF FDA UDI
- GMDN Term
- Electrocardiographic recording paper FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.2810 FDA UDI
- Commercial Distribution
- 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electrocardiographic recording paper
Vermed by Graphic Controls Acquisition Corp — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Graphic Controls Acquisition Corp
Sources (1)
- FDA UDI 74465bfa-0c7e-40b7-a3c1-24e7cec239b4 35 fields · synced Jun 1, 2026