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ESR-Vacuum tubes

FDA UDI

Class I (US FDA UDI)

by Streck

Identity

Trade Name
ESR-Vacuum tubes FDA UDI
Generic Name
Evacuated blood collection tube IVD, sodium citrate FDA UDI
Device Name
2.0ml tri-sodium citrate blood collection tubes case contains 1200 vials. FDA UDI
Model / Reference
240364 FDA UDI
Description
2.0ml tri-sodium citrate blood collection tubes case contains 1200 vials. FDA UDI

Identifiers

Catalog Number
240364 FDA UDI
Primary DI / UDI-DI
10844509000065 FDA UDI
FDA Product Code
GHC FDA UDI
GMDN Term
Evacuated blood collection tube IVD, sodium citrate FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.6700 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

Yes

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 — 2.0 Milliliter FDA UDI

Category: Evacuated blood collection tube IVD, sodium citrate

ESR-Vacuum tubes by Streck — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Evacuated blood collection tube IVD, sodium citrate.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Streck

Sources (1)

  • FDA UDI 08f0930f-b32b-4f3e-bf22-5d9ae2613e05 37 fields · synced May 29, 2026