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Seamless™

FDA UDI

Class I (US FDA UDI)

by B Braun Interventional Systems, Inc

Identity

Trade Name
Seamless™ FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
21GA X 2.5CM TW INTRO NEEDLE FDA UDI
Model / Reference
614702 FDA UDI
Description
21GA X 2.5CM TW INTRO NEEDLE FDA UDI

Identifiers

Catalog Number
614702 FDA UDI
Primary DI / UDI-DI
04046955642489 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Vascular catheter introduction set, nonimplantable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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 catheter introduction set, nonimplantable

Seamless™ by B Braun Interventional Systems, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter introduction set, nonimplantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B Braun Interventional Systems, Inc

Sources (1)

  • FDA UDI d20fa021-8687-4d07-9772-0b37d285a89b 36 fields · synced Jun 6, 2026