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Camera Drape

FDA UDI

Class II (US FDA UDI)

by Advance Medical Designs, Inc.

Identity

Trade Name
Camera Drape FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Disposable Equipment Cover FDA UDI
Model / Reference
04-CC216 FDA UDI
Description
Disposable Equipment Cover FDA UDI

Identifiers

Primary DI / UDI-DI
00848340019791 FDA UDI
510(k) Number
K850959 FDA UDI
FDA Product Code
JAA FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1650 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Medical equipment/instrument drape, single-use

Camera Drape by Advance Medical Designs, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7ce31715-1920-4deb-ac75-68f33fca05e5 34 fields · synced Jun 8, 2026