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Modification To Vascu Puncture Picc Guidewiremodification To Vascu Puncture Picc

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
MODIFICATION TO VASCU PUNCTURE PICC GUIDEWIREMODIFICATION TO VASCU PUNCTURE PICC FDA UDI
Generic Name
Peripheral vascular guidewire, manual FDA UDI
Device Name
0.018"(0.5MM)X 45CM NITINOL GUIDEWIRE WITH RADIOPAQUE TIP FDA UDI
Model / Reference
MR190045 FDA UDI
Description
0.018"(0.5MM)X 45CM NITINOL GUIDEWIRE WITH RADIOPAQUE TIP FDA UDI

Identifiers

Primary DI / UDI-DI
00884908033557 FDA UDI
FDA Product Code
DQX FDA UDI
GMDN Term
Peripheral vascular guidewire, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1330 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: Peripheral vascular guidewire, manual

Modification To Vascu Puncture Picc Guidewiremodification To Vascu Puncture Picc by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Peripheral vascular guidewire, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Components Inc

Sources (1)

  • FDA UDI 20306ea6-c4a5-4e70-8a16-8d3b671ab762 34 fields · synced Jun 8, 2026