Identity
- Trade Name
- Disc Filter FDA UDI
- Generic Name
- Hydrophobic Luer filter FDA UDI
- Model / Reference
- B00130001 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04719875918087 FDA UDI
- FDA Product Code
- JRL FDA UDI
- GMDN Term
- Hydrophobic Luer filter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2050 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
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Hydrophobic Luer filter
Disc Filter by Aeon Biotherapeutics Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Hydrophobic Luer filter.
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- LUER LOCK DISC FILTER (FEMALE TO MALE) — FLEXICARE MEDICAL LIMITED · Class I
- LUER LOCK DISC FILTER (MALE TO FEMALE) — FLEXICARE MEDICAL LIMITED · Class I
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
- Aeon Biotherapeutics Corp.
Sources (1)
- FDA UDI 89f81b40-4fd6-4140-9f03-fe1a88b08dea 32 fields · synced Jun 8, 2026