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Keystone Bartels FlexTrans Transport Medium 3mL Tube 1800pcs

FDA UDI

Class I (US FDA UDI)

by Keystone Manufacturing

Identity

Trade Name
Keystone Bartels FlexTrans Transport Medium 3mL Tube 1800pcs FDA UDI
Generic Name
General tissue specimen container IVD, fixative/saline FDA UDI
Device Name
Bartels FlexTrans Transport Medium 3mL Tube 1800pcs FDA UDI
Model / Reference
KMVIAL-VTM3ML-1800 FDA UDI
Description
Bartels FlexTrans Transport Medium 3mL Tube 1800pcs FDA UDI

Identifiers

Primary DI / UDI-DI
00860005748327 FDA UDI
FDA Product Code
KDT FDA UDI
GMDN Term
General tissue specimen container IVD, fixative/saline 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General tissue specimen container IVD, fixative/saline

Keystone Bartels FlexTrans Transport Medium 3mL Tube 1800pcs by Keystone Manufacturing — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General tissue specimen container IVD, fixative/saline.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 792077ab-5ad2-43bb-86b2-6570e2db895c 33 fields · synced Jun 6, 2026