Surshield

FDA UDI

Class II (US FDA UDI)

by Terumo Medical Products (Hangzhou) Co., Ltd.

Identity

Trade Name: SURSHIELD FDA UDI
Generic Name: Basic intravenous administration set, invasive FDA UDI
Device Name: SURSHIELD Safety Winged Infusion Set FDA UDI
Model / Reference: SV*S25BLS FDA UDI
Description: SURSHIELD Safety Winged Infusion Set FDA UDI

Identifiers

Catalog Number: SV*S25BLS FDA UDI
Primary DI / UDI-DI: 36927675504013 FDA UDI
FDA Product Code: FPA FDA UDI
GMDN Term: Basic intravenous administration set, invasive FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5440 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

Dimensions & Sizes

Size: Needle Gauge — 25 Gauge FDA UDI
Length — 0.75 Inch FDA UDI
Total Volume — 0.19 Milliliter FDA UDI

Category: Basic intravenous administration set, invasive

Surshield by Terumo Medical Products (Hangzhou) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic intravenous administration set, invasive.

Vacuette — Greiner Bio-One GmbH · Class II
SURFLO™ — Terumo Europe NV · Class II
SURFLO™ — Terumo Europe NV · Class II
VACUETTE — Greiner Bio-One GmbH · Class II
ULTRAFLO-R — Innovative Medical Technologies, Inc. · Class II
Vacuette — Greiner Bio-One GmbH · Class II
Vacuette — Greiner Bio-One GmbH · Class II
ULTRAFLO-S — Innovative Medical Technologies, 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: Terumo Medical Products (Hangzhou) Co., Ltd.

Sources (1)

FDA UDI 472056c8-a911-490d-a026-7144338f9cf9 37 fields · synced Jun 1, 2026