Identity
- Trade Name
- Boekel Blood Collection Mixer FDA UDI
- Generic Name
- Blood donation rocker FDA UDI
- Device Name
- Device used for the collection of blood combined with a mixing motion. FDA UDI
- Model / Reference
- 302000 FDA UDI
- Description
- Device used for the collection of blood combined with a mixing motion. FDA UDI
Identifiers
- Catalog Number
- 302000 FDA UDI
- Primary DI / UDI-DI
- 00863626000270 FDA UDI
- FDA Product Code
- KSQ FDA UDI
- GMDN Term
- Blood donation rocker FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.9195 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
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
No
FDA UDI
Category: Blood donation rocker
Boekel Blood Collection Mixer by Boekel Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- COMPOGUARD Advance COMPLETE — Fresenius Kabi · Class I
- Blood Collection Mixer CM735A — CENTRON CORPORATION · Class I
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
- Boekel Industries, Inc.
Sources (1)
- FDA UDI 89d0e494-544e-4899-ad5b-f6492402daf8 34 fields · synced May 30, 2026