Micro tube 2ml, PP

FDA UDI

Class I (US FDA UDI)

by Sarstedt Aktiengesellschaft & Co.KG

Identity

Trade Name: Micro tube 2ml, PP FDA UDI
Generic Name: Assay container IVD, single-use FDA UDI
Model / Reference: 72.708 FDA UDI

Identifiers

Catalog Number: 72.708 FDA UDI
Primary DI / UDI-DI: 04038917083584 FDA UDI
FDA Product Code: NNK FDA UDI
GMDN Term: Assay container IVD, single-use 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Assay container IVD, single-use

Micro tube 2ml, PP by Sarstedt Aktiengesellschaft & Co.KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Sarstedt Aktiengesellschaft & Co.KG

Sources (1)

FDA UDI 9dab23f5-7489-4de3-a3ad-970c6e17f4ac 34 fields · synced May 31, 2026