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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
ENT surgical drape FDA UDI
Device Name
DRAPE EENT SPLIT 77 X 110 FDA UDI
Model / Reference
SPT-5590SCS FDA UDI
Description
DRAPE EENT SPLIT 77 X 110 FDA UDI

Identifiers

Catalog Number
SPT-5590SCS FDA UDI
Primary DI / UDI-DI
10884389030585 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
ENT surgical drape 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

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

No

FDA UDI

Category: ENT surgical drape

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

Similar devices

Also classified as ENT surgical drape.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7cd3e5bb-8bab-4832-a986-ad27eb048376 35 fields · synced May 30, 2026