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Stryker Air

FDA UDI

Class II (US FDA UDI)

by Tridien Medical

Identity

Trade Name
Stryker Air FDA UDI
Generic Name
Low-air-loss bed FDA UDI
Device Name
HV,Intl,AfterMarket,Contrl, IA FDA UDI
Model / Reference
2861 FDA UDI
Description
HV,Intl,AfterMarket,Contrl, IA FDA UDI

Identifiers

Catalog Number
60SM-5004 FDA UDI
Primary DI / UDI-DI
00841965103197 FDA UDI
FDA Product Code
IOQ FDA UDI
GMDN Term
Low-air-loss bed 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Low-air-loss bed

Stryker Air by Tridien Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Low-air-loss bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tridien Medical

Sources (1)

  • FDA UDI f56b17d5-3fb4-4eaa-89fc-d665abd500ab 35 fields · synced Jun 1, 2026