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Accelerate II Bone Marrow Concentrating System 120mL

FDA UDI

Class I (US FDA UDI)

by EmCyte Corporation

Identity

Trade Name
Accelerate II Bone Marrow Concentrating System 120mL FDA UDI
Generic Name
Haematological concentrate system preparation kit, bone marrow concentration FDA UDI
Model / Reference
620-32-36 FDA UDI

Identifiers

Catalog Number
620-32-36 FDA UDI
Primary DI / UDI-DI
00855306003275 FDA UDI
510(k) Number
K070666 FDA UDI
FDA Product Code
JQC FDA UDI
GMDN Term
Haematological concentrate system preparation kit, bone marrow concentration FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Haematological concentrate system preparation kit, platelet concentrationHaematological concentrate system preparation kit, bone marrow concentration

Accelerate II Bone Marrow Concentrating System 120mL by EmCyte Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haematological concentrate system preparation kit, bone marrow concentration.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
EmCyte Corporation

Sources (1)

  • FDA UDI 5314956a-4d63-462f-b83d-35f89667303f 36 fields · synced Jun 9, 2026