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Medcomp Vessel Dilatormedcomp Vessel Dilator

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
MEDCOMP VESSEL DILATORMEDCOMP VESSEL DILATOR FDA UDI
Generic Name
Vascular dilator, single-use FDA UDI
Device Name
6F VESSEL DILATOR6F VESSEL DILAT (15CM / 0.038")(15CM / 0.038") FDA UDI
Model / Reference
MCD76 FDA UDI
Description
6F VESSEL DILATOR6F VESSEL DILAT (15CM / 0.038")(15CM / 0.038") FDA UDI

Identifiers

Catalog Number
MCD76 FDA UDI
Primary DI / UDI-DI
00884908127287 FDA UDI
FDA Product Code
DRE FDA UDI
GMDN Term
Vascular dilator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1310 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: Vascular dilator, single-use

Medcomp Vessel Dilatormedcomp Vessel Dilator by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular dilator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2a55ba2d-d394-4f15-baf7-2ea37dc5710b 35 fields · synced May 30, 2026