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Tunnelertunneler

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
TUNNELERTUNNELER FDA UDI
Generic Name
Vascular graft tunneller FDA UDI
Device Name
2-BARBED TUNNELERS FOR2-BARBED T 6F PRO-LINE® FDA UDI
Model / Reference
DMRACC6DTUN FDA UDI
Description
2-BARBED TUNNELERS FOR2-BARBED T 6F PRO-LINE® FDA UDI

Identifiers

Catalog Number
DMRACC6DTUN FDA UDI
Primary DI / UDI-DI
00884908142075 FDA UDI
FDA Product Code
MZY FDA UDI
GMDN Term
Vascular graft tunneller FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3450 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

Yes

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 graft tunneller

Tunnelertunneler by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular graft tunneller.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1f35e336-7cf1-4ace-b5fd-1c4f57bb279c 35 fields · synced Jun 8, 2026