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Recombinant Factor VIII Substrate, Porcine Sequence

FDA UDI

Class II (US FDA UDI)

by Takeda Pharmaceuticals U.S.A., Inc.

Identity

Trade Name
Recombinant Factor VIII Substrate, Porcine Sequence FDA UDI
Generic Name
Coagulation factor VIII IVD, antibody FDA UDI
Model / Reference
6521753 FDA UDI

Identifiers

Catalog Number
6521753 FDA UDI
Primary DI / UDI-DI
00198815000107 FDA UDI
FDA Product Code
GGC FDA UDI
GMDN Term
Coagulation factor VIII IVD, antibody FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5425 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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: Coagulation factor VIII IVD, antibody

Recombinant Factor VIII Substrate, Porcine Sequence by Takeda Pharmaceuticals U.S.A., Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Coagulation factor VIII IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2068ec62-b067-458a-a1d7-b6f7d10474e0 34 fields · synced Jun 8, 2026