Identity
- Trade Name
- Pall LeukoGuard LGB FDA UDI
- Generic Name
- Cardiopulmonary bypass system filter, arterial blood line FDA UDI
- Device Name
- Pall LeukoGuard LGB Arterial Line Leukocyte Reduction Filter with Bypass Loop FDA UDI
- Model / Reference
- LGB FDA UDI
- Description
- Pall LeukoGuard LGB Arterial Line Leukocyte Reduction Filter with Bypass Loop FDA UDI
Identifiers
- Catalog Number
- LGB FDA UDI
- Primary DI / UDI-DI
- 05034480004055 FDA UDI
- FDA Product Code
- DTM FDA UDI
- GMDN Term
- Cardiopulmonary bypass system filter, arterial blood line FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4260 FDA UDI
- Commercial Distribution
- Not 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
Ethylene Oxide FDA UDI
Dimensions & Sizes
- Size
- Pore Size — 40 Micrometer FDA UDI
Pall LeukoGuard LGB by Global Life Sciences Solutions USA LLC — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Global Life Sciences Solutions USA LLC
Sources (1)
- FDA UDI a75be26c-1b98-4cc1-8d5f-16e3e97d83f8 37 fields · synced May 30, 2026