← Back to catalogue

Dynatronics

FDA UDI

Class I (US FDA UDI)

by Armedica Manufacturing Corp.

Identity

Trade Name
DYNATRONICS FDA UDI
Generic Name
Examination/treatment table, line-powered FDA UDI
Device Name
STEEL, ELECTRIC, BAR ACTIVATED, TWO SECTION TREATMENT TABLE WITH ADJUSTABLE BACKREST, SIDE PANELS, AND CASTERS FDA UDI
Model / Reference
RAMBA240 FDA UDI
Description
STEEL, ELECTRIC, BAR ACTIVATED, TWO SECTION TREATMENT TABLE WITH ADJUSTABLE BACKREST, SIDE PANELS, AND CASTERS FDA UDI

Identifiers

Catalog Number
RAMBA240 FDA UDI
Primary DI / UDI-DI
B866MRAMBA2401 FDA UDI
FDA Product Code
INQ FDA UDI
GMDN Term
Examination/treatment table, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3760 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Examination/treatment table, line-powered

Dynatronics by Armedica Manufacturing Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Examination/treatment table, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 46eb1294-f9c1-4abb-8967-cddee3646098 34 fields · synced May 29, 2026