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Dormia

FDA UDI

Class II (US FDA UDI)

by Coloplast A/S

Identity

Trade Name
Dormia FDA UDI
Generic Name
Urinary stone retrieval basket, single-use FDA UDI
Model / Reference
EXN934 FDA UDI

Identifiers

Catalog Number
EXN934 FDA UDI
Primary DI / UDI-DI
03600040955581 FDA UDI
FDA Product Code
FFL FDA UDI
GMDN Term
Urinary stone retrieval basket, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4680 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 120 Centimeter FDA UDI
Catheter Gauge — 1.5 French FDA UDI

Category: Urinary stone retrieval basket, single-use

Dormia by Coloplast A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urinary stone retrieval basket, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Coloplast A/S

Sources (1)

  • FDA UDI 469746c4-e327-4367-9ae0-2b24f98c08b1 36 fields · synced Jun 8, 2026