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AVID TruCustom

FDA UDI

Class II (US FDA UDI)

by Avid Medical, Inc.

Identity

Trade Name
AVID TruCustom FDA UDI
Generic Name
Urological surgical procedure kit, medicated, single-use FDA UDI
Model / Reference
WRNM038-08_0010 FDA UDI

Identifiers

Catalog Number
WRNM038-08 FDA UDI
Primary DI / UDI-DI
10809160254370 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
Urological surgical procedure kit, medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

Yes

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: Urological surgical procedure kit, medicated, single-use

A comprehensive medical device directory listing the AVID TruCustom urological surgical procedure kit, including key features, regulatory compliance, and product information.

Similar devices

Also classified as Urological surgical procedure kit, medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avid Medical, Inc.

Sources (1)

  • FDA UDI 47ec34b1-32f2-49ec-9b59-fe4df0a6f471 34 fields · synced Jul 15, 2026