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Tube 4ml, 75x12mm, LH

FDA UDI

Class I (US FDA UDI)

by Sarstedt Aktiengesellschaft & Co.KG

Identity

Trade Name
Tube 4ml, 75x12mm, LH FDA UDI
Generic Name
Non-evacuated blood collection tube IVD, anticoagulant FDA UDI
Model / Reference
36.336.100 FDA UDI

Identifiers

Catalog Number
36.336.100 FDA UDI
Primary DI / UDI-DI
04038917105521 FDA UDI
FDA Product Code
PPM FDA UDI
GMDN Term
Non-evacuated blood collection tube IVD, anticoagulant FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 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: Non-evacuated blood collection tube IVD, anticoagulant

Tube 4ml, 75x12mm, LH by Sarstedt Aktiengesellschaft & Co.KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-evacuated blood collection tube IVD, anticoagulant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9501f360-a761-44ed-883d-a5f43b906ff0 34 fields · synced Jun 8, 2026