← Back to catalogue

Smr Maxi Cabinet, Aluminum Composite, Deluxe, Corded Otoscopes 220-240v, Require

FDA UDI

Class I (US FDA UDI)

by Global Surgical Corp.

Identity

Trade Name
SMR MAXI CABINET, ALUMINUM COMPOSITE, DELUXE, CORDED OTOSCOPES 220-240V, REQUIRE FDA UDI
Generic Name
ENT cabinet FDA UDI
Model / Reference
S 178000D-230 FDA UDI

Identifiers

Primary DI / UDI-DI
00810040252655 FDA UDI
FDA Product Code
ETF FDA UDI
GMDN Term
ENT cabinet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.5300 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

Smr Maxi Cabinet, Aluminum Composite, Deluxe, Corded Otoscopes 220-240v, Require by Global Surgical Corp. — Class I — FDA UDI — listed in FDA GUDID

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

Manufacturer
Global Surgical Corp.

Sources (1)

  • FDA UDI 29541f7f-2db6-4761-817f-508165e91f35 33 fields · synced Jun 1, 2026