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ProV-Access Vascular Access Needle Guide Probe Cover Kit

FDA UDI

Class II (US FDA UDI)

by Protek Medical Products, Inc.

Identity

Trade Name
ProV-Access Vascular Access Needle Guide Probe Cover Kit FDA UDI
Generic Name
Cable/lead/sensor/probe cover, sterile FDA UDI
Model / Reference
5416 FDA UDI

Identifiers

Catalog Number
5416 FDA UDI
Primary DI / UDI-DI
00841912101412 FDA UDI
510(k) Number
K970889 FDA UDI
K973958 FDA UDI
FDA Product Code
KKX FDA UDI
ITX FDA UDI
GMDN Term
Cable/lead/sensor/probe cover, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
892.1570 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

Category: Needle guide, single-useCable/lead/sensor/probe cover, sterile

ProV-Access Vascular Access Needle Guide Probe Cover Kit by Protek Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Cable/lead/sensor/probe cover, sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ae5587e2-f021-4378-91f8-8c1018f352ab 34 fields · synced May 30, 2026