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Coulmed

FDA UDI

Class II (US FDA UDI)

by Coulmed Products Group Llc

Identity

Trade Name
Coulmed FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Covex Sterile C-Arm Drape with Elastic Bands: 41" x 74" FDA UDI
Model / Reference
DI-5419 FDA UDI
Description
Covex Sterile C-Arm Drape with Elastic Bands: 41" x 74" FDA UDI

Identifiers

Catalog Number
DI-5419 FDA UDI
Primary DI / UDI-DI
10810087350076 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Medical equipment/instrument drape, 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical equipment/instrument drape, single-use

Coulmed by Coulmed Products Group Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e8bf237b-4398-4d1a-a4c6-2fe4e987df0c 34 fields · synced Jun 8, 2026