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Delta

FDA UDI

Class I (US FDA UDI)

by Stryker Leibinger

Identity

Trade Name
DELTA FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
DELTA 1.7MM INSTRUMENT MODULE FDA UDI
Model / Reference
70-71702 FDA UDI
Description
DELTA 1.7MM INSTRUMENT MODULE FDA UDI

Identifiers

Catalog Number
70-71702 FDA UDI
Primary DI / UDI-DI
07613252272861 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Device sterilization/disinfection container, reusable

Delta by Stryker Leibinger — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Leibinger

Sources (1)

  • FDA UDI f4253a44-e9c4-4cdb-b98e-e04ed8c0f615 34 fields · synced May 30, 2026