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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Blood collection tube holder, single-use FDA UDI
Device Name
TUBE,CENT,STR,BAG,PREM,SEAL RING,15M FDA UDI
Model / Reference
MLAB15013 FDA UDI
Description
TUBE,CENT,STR,BAG,PREM,SEAL RING,15M FDA UDI

Identifiers

Catalog Number
MLAB15013 FDA UDI
Primary DI / UDI-DI
20197344006097 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Blood collection tube holder, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

Yes

FDA UDI

Category: Blood collection tube holder, single-use

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood collection tube holder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5c70b16b-25b4-480e-84ae-756f7b6232c4 35 fields · synced Jun 8, 2026