← Back to catalogue

Cyto-Tek®

FDA UDI

Class I (US FDA UDI)

by Sakura Finetek USA, Inc

Identity

Trade Name
Cyto-Tek® FDA UDI
Generic Name
Specimen container mailer, insulated FDA UDI
Device Name
Mailer FDA UDI
Model / Reference
4310 FDA UDI
Description
Mailer FDA UDI

Identifiers

Catalog Number
4310 FDA UDI
Primary DI / UDI-DI
00615233078438 FDA UDI
FDA Product Code
KDT FDA UDI
GMDN Term
Specimen container mailer, insulated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Specimen container mailer, insulated

Cyto-Tek® by Sakura Finetek USA, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Specimen container mailer, insulated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI bd535d40-4256-4884-8a1b-dcaedff86787 35 fields · synced Jun 8, 2026