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Teco Diagnostics Glucose (Hexokinase) Liquid Reagent
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Teco Diagnostics Glucose (Hexokinase) Liquid Reagent FDA UDI
- Generic Name
- Glucose IVD, reagent FDA UDI
- Device Name
- Teco Diagnostics Glucose (Hexokinase) Liquid Reagent is used for the in vitro quantitative determination of glucose in human serum or plasma. FDA UDI
- Model / Reference
- G516-150 FDA UDI
- Description
- Teco Diagnostics Glucose (Hexokinase) Liquid Reagent is used for the in vitro quantitative determination of glucose in human serum or plasma. FDA UDI
Identifiers
- Catalog Number
- G516-150 FDA UDI
- Primary DI / UDI-DI
- 10673486001662 FDA UDI
- 510(k) Number
- K000102 FDA UDI
- FDA Product Code
- CFR FDA UDI
- GMDN Term
- Glucose IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1345 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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: Glucose IVD, reagent
Teco Diagnostics Glucose (Hexokinase) Liquid Reagent by Teco Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Teco Diagnostics
Sources (1)
- FDA UDI db9429e3-08eb-4cf4-ac4a-8b1931af1c3b 37 fields · synced Jun 8, 2026