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N/An/A

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
N/AN/A FDA UDI
Generic Name
Subcutaneous tunneller, single-use FDA UDI
Device Name
HEMO-CATH®BLUNT TROCAR W/SLEEVEW/SLEEVE FDA UDI
Model / Reference
DBTH FDA UDI
Description
HEMO-CATH®BLUNT TROCAR W/SLEEVEW/SLEEVE FDA UDI

Identifiers

Catalog Number
DBTH FDA UDI
Primary DI / UDI-DI
00884908145649 FDA UDI
FDA Product Code
DRC FDA UDI
GMDN Term
Subcutaneous tunneller, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1390 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: Subcutaneous tunneller, single-use

N/An/A by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Subcutaneous tunneller, single-use.

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 23162fa1-c6dc-41c9-a16c-a92819a873d5 35 fields · synced May 30, 2026