CentroVena

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name: CentroVena FDA UDI
Generic Name: Central venous catheterization kit, short-term FDA UDI
Device Name: Acute Central Venous Catheter, Dual Lumen, Soft Tip, 7 F (2.5 mm OD) X 16 cm FDA UDI
Model / Reference: 1MB07216 FDA UDI
Description: Acute Central Venous Catheter, Dual Lumen, Soft Tip, 7 F (2.5 mm OD) X 16 cm FDA UDI

Identifiers

Catalog Number: 1MB07216 FDA UDI
Primary DI / UDI-DI: 00801741202254 FDA UDI
FDA Product Code: FOZ FDA UDI
GMDN Term: Central venous catheterization kit, short-term FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Dimensions & Sizes

Size: Length — 16 Centimeter FDA UDI
Catheter Gauge — 7 French FDA UDI

Category: Central venous catheterization kit, short-term

CentroVena by Bard Access Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Acent-1 — Global Medikit Limited · Class III
Centurion — Centurion Medical Products · Class II
MEDLINE — MEDLINE INDUSTRIES, INC. · Class II
Cook — COOK INCORPORATED · Class II
Shun Monitor® — Shunmei Medical Co.,Ltd · Class III
ARROW — TELEFLEX INCORPORATED · Class II
Medline Industries, Inc. — Centurion Medical Products · Class II
MEDLINE — MEDLINE INDUSTRIES, INC. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: Bard Access Systems, Inc.

Sources (1)

FDA UDI d303c014-887f-47f2-81fb-3d1faad2f8a5 37 fields · synced Jun 9, 2026