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TotalExam® 3.2 Camera

FDA UDI

Class I (US FDA UDI)

by GlobalMed Holdings, LLC

Identity

Trade Name
TotalExam® 3.2 Camera FDA UDI
Generic Name
Multi-purpose digital medical camera FDA UDI
Device Name
TotalExam® 3.2.1 Examination Camera w/ Otoscope & Auto Focus Lens Attachments. FDA UDI
Model / Reference
GMD5504HD58 FDA UDI
Description
TotalExam® 3.2.1 Examination Camera w/ Otoscope & Auto Focus Lens Attachments. FDA UDI

Identifiers

Catalog Number
GMD5504HD58 FDA UDI
Primary DI / UDI-DI
00850033167009 FDA UDI
FDA Product Code
KZF FDA UDI
GMDN Term
Multi-purpose digital medical camera FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6320 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: Multi-purpose digital medical camera

TotalExam® 3.2 Camera by GlobalMed Holdings, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose digital medical camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cc2bac1e-6252-48e3-9350-60c7842f361f 34 fields · synced Jun 9, 2026