Surshield

FDA UDI

Class II (US FDA UDI)

by Terumo Corp.

Identity

Trade Name: SURSHIELD FDA UDI
Generic Name: Peripheral intravenous cannula FDA UDI
Device Name: SURSHIELD-PUR SAFETY I.V.Catheter FDA UDI
Model / Reference: SR*SFF2032A FDA UDI
Description: SURSHIELD-PUR SAFETY I.V.Catheter FDA UDI

Identifiers

Primary DI / UDI-DI: 34987350705663 FDA UDI
FDA Product Code: FOZ FDA UDI
GMDN Term: Peripheral intravenous cannula 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

FDA UDI

Combination Product

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 Unsafe FDA UDI

Dimensions & Sizes

Size: Lumen/Inner Diameter — 0.8 Millimeter FDA UDI
Catheter Gauge — 20 French FDA UDI
Length — 1.25 Inch FDA UDI
Outer Diameter — 1.1 Millimeter FDA UDI

Category: Peripheral intravenous cannula

Surshield by Terumo Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral intravenous cannula.

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Navilyst Medical — NAVILYST MEDICAL, INC.
McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class II
Navilyst Medical — NAVILYST MEDICAL, INC.
McKesson — MCKESSON MEDICAL-SURGICAL 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

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Manufacturer

Manufacturer: Terumo Corp.

Sources (1)

FDA UDI e1f47c8b-b488-4348-a06b-0015239fe2dd 36 fields · synced May 30, 2026