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Transmedics

FDA UDI

Class II (US FDA UDI)

by Tidi Products, Llc

Identity

Trade Name
Transmedics FDA UDI
Generic Name
Urological fluid funnel FDA UDI
Device Name
Transmedics Equipment Covers Clear Polyethylene 55in x 66in x 1in 12 per Case FDA UDI
Model / Reference
32674 FDA UDI
Description
Transmedics Equipment Covers Clear Polyethylene 55in x 66in x 1in 12 per Case FDA UDI

Identifiers

Primary DI / UDI-DI
01618125152147 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
Urological fluid funnel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Transmedics by Tidi Products, Llc — 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

Manufacturer
Tidi Products, Llc

Sources (1)

  • FDA UDI 8bc74d20-00fe-4155-877e-05aef4c63bfe 34 fields · synced May 30, 2026