← Back to catalogue

Medline Industries, Inc.

FDA UDI

Class II (US FDA UDI)

by Centurion Medical Products

Identity

Trade Name
Medline Industries, Inc. FDA UDI
Generic Name
Central venous catheterization kit, short-term FDA UDI
Device Name
VANTEX 7FR 3L 20CM CVC BUNDLE FDA UDI
Model / Reference
ECVC6505 FDA UDI
Description
VANTEX 7FR 3L 20CM CVC BUNDLE FDA UDI

Identifiers

Catalog Number
ECVC6505 FDA UDI
Primary DI / UDI-DI
10653160336327 FDA UDI
FDA Product Code
OES FDA UDI
GMDN Term
Central venous catheterization kit, short-term FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 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

Yes

FDA UDI

Combination Product

Yes

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: Central venous catheterization kit, short-term

Medline Industries, Inc. by Centurion Medical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Central venous catheterization kit, short-term.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b53838fc-6cf3-40bb-9a82-6159fe597943 35 fields · synced May 31, 2026