AccessGUDID - DEVICE: ARMEDICA (B866MAMTMBA5001)

GUDID

Device Identifier (DI) Information

Brand Name: ARMEDICA
Version or Model: AMTMBA500
Commercial Distribution Status: In Commercial Distribution
Catalog Number: AMTMBA500
Company Name: ARMEDICA MANUFACTURING CORP.

Primary DI Number: B866MAMTMBA5001
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 018941711 *Terms of Use

Device Description: Steel, electrical, bar activated, 3 section treatment table, 27 inches wide, adjustable 3 piece head section, adjustable center and foot sections with locking casters

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
31362	Examination/treatment table, line-powered	A mobile, mains electricity (AC-powered) motorized table designed for routine/minor medical examinations and/or treatment of the patient. It will typically consist of a framework or a large pedestal with a flat table top surface which consists of some articulated sections that can be adjusted into a raised position. The height of the table top surface will also be power-adjusted. It is typically used in examination rooms, endoscopy facilities, electrophysiology (EP) laboratories, or outpatient departments for minor interventions.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
INQ	Table, Powered

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 4aee076a-da9e-440b-b07f-3b34d85ed73e
Public Version Date: December 16, 2024
Public Version Number: 1
DI Record Publish Date: December 06, 2024