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IsoFlex LAL

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
IsoFlex LAL FDA UDI
Generic Name
Gel-filled bed mattress FDA UDI
Model / Reference
2860 FDA UDI

Identifiers

Catalog Number
2860-000-011 FDA UDI
Primary DI / UDI-DI
07613327277739 FDA UDI
FDA Product Code
IOQ FDA UDI
GMDN Term
Gel-filled bed mattress FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5170 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gel-filled bed mattress

IsoFlex LAL by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gel-filled bed mattress.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI ba132ed4-3f87-4ca6-bc8c-ec1ed90bf276 34 fields · synced Jun 1, 2026