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Tube 25ml 90x25PP+Cap

FDA UDI

Class I (US FDA UDI)

by Sarstedt Aktiengesellschaft & Co.KG

Identity

Trade Name
Tube 25ml 90x25PP+Cap FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Model / Reference
60.9922.243 FDA UDI

Identifiers

Catalog Number
60.9922.243 FDA UDI
Primary DI / UDI-DI
04038917151528 FDA UDI
FDA Product Code
KDT FDA UDI
GMDN Term
General specimen container IVD, no additive/medium 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

Yes

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: General specimen container IVD, no additive/medium

Tube 25ml 90x25PP+Cap by Sarstedt Aktiengesellschaft & Co.KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, no additive/medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sarstedt Aktiengesellschaft & Co.KG

Sources (1)

  • FDA UDI adc4f6da-a150-443f-8890-117dfc1a345f 34 fields · synced Jun 7, 2026