Identity
- Trade Name
- BD MiniDraw™ H&H Capillary Blood Collection Tube FDA UDI
- Generic Name
- Capillary blood collection tube IVD, no additive FDA UDI
- Device Name
- BD MiniDraw™ H&H Capillary Blood Collection Tube FDA UDI
- Model / Reference
- 366603 FDA UDI
- Description
- BD MiniDraw™ H&H Capillary Blood Collection Tube FDA UDI
Identifiers
- Catalog Number
- 366603 FDA UDI
- Primary DI / UDI-DI
- 50382903666039 FDA UDI
- 510(k) Number
- K230493 FDA UDI
- FDA Product Code
- GIM FDA UDI
- GMDN Term
- Capillary blood collection tube IVD, no additive FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1675 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
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
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 425 Microliter FDA UDI
Category: Capillary blood collection tube IVD, no additive
BD MiniDraw™ H&H Capillary Blood Collection Tube by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K230493 also covers:
- BD MiniDraw™ Capillary Tube Adapter H&H — BECTON DICKINSON AND COMPANY
- BD MiniDraw™ Finger Sizing Tool — BECTON DICKINSON AND COMPANY
- BD MiniDraw™ Finger Sleeve, Extra-Large — BECTON DICKINSON AND COMPANY
- BD MiniDraw™ Finger Sleeve, Large — BECTON DICKINSON AND COMPANY
- BD MiniDraw™ Finger Sleeve, Medium — BECTON DICKINSON AND COMPANY
- BD MiniDraw™ Finger Sleeve, Small — BECTON DICKINSON AND COMPANY
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Becton Dickinson And Company
Sources (1)
- FDA UDI 95972fce-2b9d-46b2-a6c2-5068da91fb39 37 fields · synced Jun 1, 2026