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Haemonetics

FDA UDI

Class II (US FDA UDI)

by Haemonetics Corporation

Identity

Trade Name
Haemonetics FDA UDI
Generic Name
Blood/tissue storage/culture container FDA UDI
Device Name
Transfer Bag 600 ml w/Y set FDA UDI
Model / Reference
732-33M FDA UDI
Description
Transfer Bag 600 ml w/Y set FDA UDI

Identifiers

Primary DI / UDI-DI
20887691002858 FDA UDI
FDA Product Code
KSR FDA UDI
GMDN Term
Blood/tissue storage/culture container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9100 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

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 — 600 Milliliter FDA UDI

Category: Blood/tissue storage/culture container

Haemonetics by Haemonetics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood/tissue storage/culture container.

Cleared under the same submission

BK840010 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Haemonetics Corporation

Sources (1)

  • FDA UDI be954e4d-30b3-48f6-909b-7c73c9c7f71a 36 fields · synced Jun 8, 2026