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BD PosiFlush

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD PosiFlush FDA UDI
Generic Name
Vascular catheter flush syringe FDA UDI
Device Name
HEPARIN 10UL 2ML FILL IN 3ML SYRINGE FDA UDI
Model / Reference
306527 FDA UDI
Description
HEPARIN 10UL 2ML FILL IN 3ML SYRINGE FDA UDI

Identifiers

Catalog Number
306527 FDA UDI
Primary DI / UDI-DI
30382903065272 FDA UDI
510(k) Number
K011967 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Vascular catheter flush syringe 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

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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vascular catheter flush syringe

BD PosiFlush by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter flush syringe.

Cleared under the same submission

K011967 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI 9c5a5a92-3d98-488e-8414-60835781d7f6 36 fields · synced May 29, 2026