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Symetrex Tm

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
SYMETREX TM FDA UDI
Generic Name
Double-lumen haemodialysis catheter, implantable FDA UDI
Device Name
15.5F X 28CM SYMETREX KIT (CUFF 28CM FROM TIP) FDA UDI
Model / Reference
MS20028 FDA UDI
Description
15.5F X 28CM SYMETREX KIT (CUFF 28CM FROM TIP) FDA UDI

Identifiers

Primary DI / UDI-DI
00884908126327 FDA UDI
FDA Product Code
MSD FDA UDI
GMDN Term
Double-lumen haemodialysis catheter, implantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5540 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Symetrex Tm 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 2c6133d4-fd6a-4602-bbda-ed68263c031d 35 fields · synced May 30, 2026