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Sterile-Z

FDA UDI

Class II (US FDA UDI)

by Tidi Products, Llc

Identity

Trade Name
Sterile-Z FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Patient Drape FDA UDI
Model / Reference
5574NS FDA UDI
Description
Patient Drape FDA UDI

Identifiers

Catalog Number
5574NS FDA UDI
Primary DI / UDI-DI
10618125189394 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

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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Medical equipment/instrument drape, single-use

Sterile-Z by Tidi Products, 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

Manufacturer
Tidi Products, Llc

Sources (1)

  • FDA UDI 30969f1e-9ef9-41f7-b268-c6a75fe2560f 34 fields · synced Jun 6, 2026