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BD Vacutainer® EST™ Blood Collection Tube

FDA UDI

Class I (US FDA UDI)

by Becton, Dickinson U.K. Limited

Identity

Trade Name
BD Vacutainer® EST™ Blood Collection Tube FDA UDI
Generic Name
Evacuated blood collection tube IVD, no additive FDA UDI
Device Name
TUBE EST PLH 13X75 3.0 SLBLCE NAT FDA UDI
Model / Reference
362725 FDA UDI
Description
TUBE EST PLH 13X75 3.0 SLBLCE NAT FDA UDI

Identifiers

Catalog Number
362725 FDA UDI
Primary DI / UDI-DI
30382903627258 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
Evacuated blood collection tube IVD, no additive 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

Yes

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: Evacuated blood collection tube IVD, no additive

BD Vacutainer® EST™ Blood Collection Tube by Becton, Dickinson U.K. Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Evacuated blood collection tube IVD, no additive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Becton, Dickinson U.K. Limited

Sources (1)

  • FDA UDI 6694b912-bc00-490d-8de6-0f6233eb5e00 35 fields · synced Jun 1, 2026