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Kavowerk Dentale Einrichtungen

FDA UDI

Class I (US FDA UDI)

by Tidi Products, Llc

Identity

Trade Name
Kavowerk Dentale Einrichtungen FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Camera Covers Clear Polyethylene 500 per Box FDA UDI
Model / Reference
20926 FDA UDI
Description
Camera Covers Clear Polyethylene 500 per Box FDA UDI

Identifiers

Catalog Number
1.002.9067 FDA UDI
Primary DI / UDI-DI
00618125119202 FDA UDI
FDA Product Code
KQM FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 FDA UDI
Commercial Distribution
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

Yes

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

Yes

FDA UDI

Category: Medical equipment/instrument drape, single-use

Kavowerk Dentale Einrichtungen by Tidi Products, Llc — Class I — 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

Manufacturer
Tidi Products, Llc

Sources (1)

  • FDA UDI c8fd2570-7840-4d9f-ab2e-12b11d402e66 34 fields · synced Jun 8, 2026