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Accessories

FDA UDI

Class I (US FDA UDI)

by OriGen Biomedical, Inc.

Identity

Trade Name
Accessories FDA UDI
Generic Name
Blood transfer set FDA UDI
Device Name
One spike to one spike port and two female luers with 12cm SCD tubing and pinch clamps FDA UDI
Model / Reference
S-FFP12 FDA UDI
Description
One spike to one spike port and two female luers with 12cm SCD tubing and pinch clamps FDA UDI

Identifiers

Catalog Number
S-FFP12 FDA UDI
Primary DI / UDI-DI
10816203023985 FDA UDI
FDA Product Code
KJG FDA UDI
GMDN Term
Blood transfer set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3010 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood transfer set

Accessories by OriGen Biomedical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood transfer set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1989b9fb-9a6e-453f-bcb1-e1b2daab2311 36 fields · synced May 30, 2026