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Apex 2312 Exam Chair With Motorized Lift, Manual Backrest/Calfrest Recline, Arti

FDA UDI

Class I (US FDA UDI)

by Global Surgical Corp.

Identity

Trade Name
APEX 2312 EXAM CHAIR WITH MOTORIZED LIFT, MANUAL BACKREST/CALFREST RECLINE, ARTI FDA UDI
Generic Name
ENT chair, electric FDA UDI
Model / Reference
S 231200 FDA UDI

Identifiers

Primary DI / UDI-DI
00810040253379 FDA UDI
FDA Product Code
FRK FDA UDI
GMDN Term
ENT chair, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6140 FDA UDI
Commercial Distribution
Not 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

Yes

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

Apex 2312 Exam Chair With Motorized Lift, Manual Backrest/Calfrest Recline, Arti by Global Surgical Corp. — Class I — FDA UDI — listed in FDA GUDID

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Global Surgical Corp.

Sources (1)

  • FDA UDI 66d0b503-29a9-4461-89da-654035239f41 33 fields · synced May 30, 2026