Identity
- Trade Name
- Argyle FDA UDI
- Generic Name
- Instrument warmer, electric FDA UDI
- Device Name
- Infant Heel Warmer,No Attachment Tab FDA UDI
- Model / Reference
- MH00002N FDA UDI
- Description
- Infant Heel Warmer,No Attachment Tab FDA UDI
Identifiers
- Catalog Number
- MH00002N FDA UDI
- Primary DI / UDI-DI
- 30884527004625 FDA UDI
- FDA Product Code
- MPO FDA UDI
- GMDN Term
- Instrument warmer, electric FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5710 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
No
FDA UDI
Argyle by Cardinalhealth — 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
- Cardinalhealth
Sources (1)
- FDA UDI 660a09a1-c4bd-47c9-90e0-2fa965c9d410 36 fields · synced May 30, 2026