Access hLH Reagent Pack
Ref 33510
Active
CE IVDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number15099590575243 | Date23 Apr 2024 | StatusListed |
| European Union | CE/IVDR EUDAMED | Number150995901AcchLHSA 15099590575243 | Date2 May 2022 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Access hLH Reagent Pack EUDAMEDAccess hLH GUDID
- Generic Name
- Luteinizing hormone (LH) IVD, kit, chemiluminescent immunoassay
- Model / Ref / Catalog
- 33510
- Primary DI / UDI-DI
- 15099590575243
- Basic UDI-DI
- 150995901AcchLHSA
- FDA Product Code
- CEP
- EMDN Code
- W0102050105 Luteinising hormone
- GMDN Term
- Luteinizing hormone (LH) IVD, kit, chemiluminescent immunoassay
- Device Class
- Class B EUDAMEDClass I GUDID
- Regulation Number
- 862.1485
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class B | Class I |
Manufacturer details
- EUDAMED SRN
- US-MF-000010288
- Authorised representative
- Beckman Coulter Ireland Inc. IE-AR-000000886
Other devices from Beckman Coulter, Inc.
Properties
Other properties (15)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Human Tissues: No
- Microbial Substances: No
- Self Testing: No
- Near-Patient Testing: No
- Companion Diagnostics: No
- Surgical Instrument: No
- New Device: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Serial Number: No