Identity
- Trade Name
- SWINGMED FDA UDI
- Generic Name
- HLA class II antibody identification panel IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Model / Reference
- NC005 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06947656115181 FDA UDI
- FDA Product Code
- KMA FDA UDI
- GMDN Term
- HLA class II antibody identification panel IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.5550 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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: HLA class II antibody identification panel IVD, kit, enzyme immunoassay (EIA)
Swingmed by Guangzhou Berrcom Medical Device Co., Ltd — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Guangzhou Berrcom Medical Device Co., Ltd
Sources (1)
- FDA UDI 370a509f-b181-4304-950f-ad8b2b0082b2 32 fields · synced Jun 8, 2026