Identity
- Trade Name
- Span-America FDA UDI
- Generic Name
- Foam bed mattress FDA UDI
- Device Name
- PG RENEW 80X38X7 HOME USE FDA UDI
- Model / Reference
- Geomattress FDA UDI
- Description
- PG RENEW 80X38X7 HOME USE FDA UDI
Identifiers
- Catalog Number
- RW803829 FDA UDI
- Primary DI / UDI-DI
- H933RW803829 FDA UDI
- FDA Product Code
- IKY FDA UDI
- GMDN Term
- Foam bed mattress FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5150 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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Foam bed mattress
Span-America by Span-America Medical Systems, Inc. — 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
- Span-America Medical Systems, Inc.
Sources (1)
- FDA UDI 3cd0bbac-eeb1-461a-bcf5-bf676f22b32e 34 fields · synced Jun 12, 2026