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Dako

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Singapore Pte Ltd

Identity

Trade Name
Dako FDA UDI
Generic Name
Terminal deoxynucleotidyl transferase (TdT) IVD, antibody FDA UDI
Device Name
Monoclonal Mouse Anti-Human Terminal Deoxynucleotidyl Transferase/iFluor 700 Clone DAK-TDT FDA UDI
Model / Reference
IF002 FDA UDI
Description
Monoclonal Mouse Anti-Human Terminal Deoxynucleotidyl Transferase/iFluor 700 Clone DAK-TDT FDA UDI

Identifiers

Primary DI / UDI-DI
05700575002434 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
Terminal deoxynucleotidyl transferase (TdT) IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4020 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 0.5 Milliliter FDA UDI

Category: Terminal deoxynucleotidyl transferase (TdT) IVD, antibody

Dako by Agilent Technologies Singapore Pte Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Terminal deoxynucleotidyl transferase (TdT) IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 858c5196-bfa1-4bc3-878e-48b6afb7b2ba 36 fields · synced Jun 1, 2026