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Advanced Stretcher, Hand-Carried

FDA UDI

Class I (US FDA UDI)

by Advanced Instrumentations, Inc.

Identity

Trade Name
ADVANCED STRETCHER, HAND-CARRIED FDA UDI
Generic Name
Orthopaedic stretcher FDA UDI
Model / Reference
ST-100 FDA UDI

Identifiers

Primary DI / UDI-DI
B510ST1000 FDA UDI
FDA Product Code
FPP FDA UDI
GMDN Term
Orthopaedic stretcher FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6900 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

Yes

FDA UDI

Category: Orthopaedic stretcher

Advanced Stretcher, Hand-Carried by Advanced Instrumentations, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic stretcher.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9accf84f-ad69-4c0f-9d14-af5630ee81f2 33 fields · synced May 30, 2026