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Vascu-Sheath®ii

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
VASCU-SHEATH®II FDA UDI
Generic Name
Vascular catheter introduction needle FDA UDI
Device Name
6F (1.9MM ID) X 10CM6F (1.9MM ID VASCU-SHEATH®INTRODUCER SETSET FDA UDI
Model / Reference
DMPC-6 FDA UDI
Description
6F (1.9MM ID) X 10CM6F (1.9MM ID VASCU-SHEATH®INTRODUCER SETSET FDA UDI

Identifiers

Catalog Number
DMPC-6 FDA UDI
Primary DI / UDI-DI
00884908145502 FDA UDI
FDA Product Code
DYB FDA UDI
GMDN Term
Vascular catheter introduction needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1340 FDA UDI
Commercial Distribution
Not 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

Vascu-Sheath®ii by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 30249039-8fe2-4c97-a607-e235e9ee9a6f 36 fields · synced May 31, 2026