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Clear-View Subcutaneous Infusion Set

FDA UDI

Class II (US FDA UDI)

by Norfolk Medical

Identity

Trade Name
Clear-View Subcutaneous Infusion Set FDA UDI
Generic Name
Electric infusion pump administration set, single-use FDA UDI
Device Name
27G x 12mm x 24" Clear-View "Sub-Q" Infusion Set FDA UDI
Model / Reference
Clear-View "Sub-Q" FDA UDI
Description
27G x 12mm x 24" Clear-View "Sub-Q" Infusion Set FDA UDI

Identifiers

Catalog Number
CVS33330 FDA UDI
Primary DI / UDI-DI
M991CVS333301 FDA UDI
510(k) Number
K870188 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Electric infusion pump administration set, single-use 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

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

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 27 Gauge FDA UDI

Category: Electric infusion pump administration set, single-use

Clear-View Subcutaneous Infusion Set by Norfolk Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric infusion pump administration set, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Norfolk Medical

Sources (1)

  • FDA UDI 2e9e5bbb-2fa6-4725-98bd-cc3e215ed83d 37 fields · synced Jun 1, 2026