Identity
- Trade Name
- PMI FDA UDI
- Generic Name
- Fluid transfer set, general-purpose FDA UDI
- Device Name
- PMI Empty IV Bag 150 mL; 2 ports FDA UDI
- Model / Reference
- PMI150ML FDA UDI
- Description
- PMI Empty IV Bag 150 mL; 2 ports FDA UDI
Identifiers
- Catalog Number
- PMI150ML FDA UDI
- Primary DI / UDI-DI
- 00812608021710 FDA UDI
- FDA Product Code
- KPE FDA UDI
- GMDN Term
- Fluid transfer set, general-purpose FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5025 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 150 Milliliter FDA UDI
Category: Fluid transfer set, general-purpose
Pmi by Progressive Medical, 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
- Progressive Medical, Inc.
Sources (1)
- FDA UDI ccbc5353-ff97-4e1d-9708-5307a4e47005 36 fields · synced May 30, 2026