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IMMULITE® Systems TG Recovery Sample Thyroglobulin
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- IMMULITE® Systems TG Recovery Sample Thyroglobulin FDA UDI
- Generic Name
- Thyroglobulin IVD, reagent FDA UDI
- Device Name
- Thyreoglobulin Recovery Sample - IMMULITE - CONS - 80 Tests FDA UDI
- Model / Reference
- 10381639 FDA UDI
- Description
- Thyreoglobulin Recovery Sample - IMMULITE - CONS - 80 Tests FDA UDI
Identifiers
- Catalog Number
- LTYRM FDA UDI
- Primary DI / UDI-DI
- 00630414954523 FDA UDI
- 510(k) Number
- K982466 FDA UDI
- FDA Product Code
- MSW FDA UDI
- GMDN Term
- Thyroglobulin IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.6010 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Thyroglobulin IVD, reagent
IMMULITE® Systems TG Recovery Sample Thyroglobulin by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID
Cleared under the same submission
K982466 also covers:
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 |
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Manufacturer
- Manufacturer
- Siemens Healthcare Diagnostics Products Ltd
Sources (1)
- FDA UDI 245f76f9-7ce6-4478-8cfc-ed252acf4cd4 37 fields · synced May 30, 2026