Identity
- Trade Name
- SUPOR FDA UDI
- Generic Name
- Laboratory syringe filter FDA UDI
- Device Name
- 32 mm 1.2 Micron Syringe Filter FDA UDI
- Model / Reference
- H93824648 FDA UDI
- Description
- 32 mm 1.2 Micron Syringe Filter FDA UDI
Identifiers
- Catalog Number
- H93824648 FDA UDI
- Primary DI / UDI-DI
- 05413765482731 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- Laboratory syringe filter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 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
Dimensions & Sizes
- Size
- Outer Diameter — 32 Millimeter FDA UDIPore Size — 1.2 Micrometer FDA UDI
Supor by Baxter Healthcare Corp — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Baxter Healthcare Corp
Sources (1)
- FDA UDI 356a0e0b-721c-4bc0-adfc-12274e074971 37 fields · synced Jun 1, 2026