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mild Device Kit

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
mild Device Kit FDA UDI
Generic Name
Neurosurgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Device Kit FDA UDI
Model / Reference
MDK-0001 FDA UDI
Description
Device Kit FDA UDI

Identifiers

Catalog Number
MDK-0001 FDA UDI
Primary DI / UDI-DI
07613327651683 FDA UDI
510(k) Number
K093062 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Neurosurgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

Category: Neurosurgical procedure kit, non-medicated, single-use

mild Device Kit by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI b70c944c-9f49-40ac-8c98-1336ac56d48d 37 fields · synced May 31, 2026