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Sprinter XL (model 160 samples, IFA incl. incubator)
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Sprinter XL (model 160 samples, IFA incl. incubator) FDA UDI
- Generic Name
- Laboratory diluter FDA UDI
- Model / Reference
- YG 0033-0101-4 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04049016109693 FDA UDI
- FDA Product Code
- JQW FDA UDI
- GMDN Term
- Laboratory diluter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2750 FDA UDI
- Commercial Distribution
- Not 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Sprinter XL (model 160 samples, IFA incl. incubator) by EUROIMMUN Medizinische Labordiagnostika AG — Class I — FDA UDI — listed in FDA GUDID
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
- EUROIMMUN Medizinische Labordiagnostika AG
Sources (1)
- FDA UDI 81cc5be4-43e4-4c96-8419-75c6102f1056 33 fields · synced Jun 1, 2026