← Back to catalogue

Sterimed

FDA UDI

Class II (US FDA UDI)

by Sterimed, Inc.

Identity

Trade Name
Sterimed FDA UDI
Generic Name
X-ray system cover FDA UDI
Device Name
Equipment Drape 18" X 24" FDA UDI
Model / Reference
0888 FDA UDI
Description
Equipment Drape 18" X 24" FDA UDI

Identifiers

Primary DI / UDI-DI
00850341007165 FDA UDI
510(k) Number
K853044 FDA UDI
FDA Product Code
IZI FDA UDI
GMDN Term
X-ray system cover FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1600 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

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: X-ray system cover

Sterimed by Sterimed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray system cover.

Cleared under the same submission

K853044 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Sterimed, Inc.

Sources (1)

  • FDA UDI aaf33d65-9557-4614-9794-941cc13c6a16 35 fields · synced Jun 1, 2026