← Back to catalogue

Boekel Blood Collection Mixer

FDA UDI

Class I (US FDA UDI)

by Boekel Industries, Inc.

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

Similar devices

Also classified as Blood donation rocker.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 89d0e494-544e-4899-ad5b-f6492402daf8 34 fields · synced May 30, 2026