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BD PosiFlush SureScrub

FDA UDI

Class U (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD PosiFlush SureScrub FDA UDI
Generic Name
Vascular catheterization support/maintenance kit, non-medicated FDA UDI
Device Name
SYR 3ML SURESCRUB POSIFLUSH SALINE FDA UDI
Model / Reference
306557 FDA UDI
Description
SYR 3ML SURESCRUB POSIFLUSH SALINE FDA UDI

Identifiers

Catalog Number
306557 FDA UDI
Primary DI / UDI-DI
30382903065579 FDA UDI
510(k) Number
K121655 FDA UDI
FDA Product Code
LKB FDA UDI
GMDN Term
Vascular catheterization support/maintenance kit, non-medicated FDA UDI

Classification

Device Class
U 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

No

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 catheterization support/maintenance kit, non-medicated

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

Similar devices

Also classified as Vascular catheterization support/maintenance kit, non-medicated.

Cleared under the same submission

K121655 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 56d7528c-b7c5-4aa5-8abf-2be1230fc42f 36 fields · synced May 30, 2026