Identity
- Trade Name
- Microtainer® K2E Blood Collection Tubes FDA UDI
- Generic Name
- Evacuated blood collection tube IVD, anticoagulant FDA UDI
- Device Name
- TUBE MICRO W/MICROGARD EDTA LAV FDA UDI
- Model / Reference
- 365975 FDA UDI
- Description
- TUBE MICRO W/MICROGARD EDTA LAV FDA UDI
Identifiers
- Catalog Number
- 365975 FDA UDI
- Primary DI / UDI-DI
- 30382903659754 FDA UDI
- 510(k) Number
- K940905 FDA UDI
- FDA Product Code
- JKA FDA UDI
- GMDN Term
- Evacuated blood collection tube IVD, anticoagulant FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1675 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
Yes
FDA UDI
Microtainer® K2E Blood Collection Tubes by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K940905 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
- Becton Dickinson And Company
Sources (1)
- FDA UDI 2ac9e507-90c8-4630-8749-1de38572ddb1 37 fields · synced May 30, 2026