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Smr Maxi Cabinet, Aluminum Composite, Standard, Rechargeable Otoscopes, 220-240v

FDA UDI

Class I (US FDA UDI)

by Global Surgical Corp.

Identity

Trade Name
SMR MAXI CABINET, ALUMINUM COMPOSITE, STANDARD, RECHARGEABLE OTOSCOPES, 220-240V FDA UDI
Generic Name
ENT cabinet FDA UDI
Model / Reference
S 170001D-230 FDA UDI

Identifiers

Primary DI / UDI-DI
00810040252549 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, Standard, Rechargeable Otoscopes, 220-240v 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 756be670-d444-4b74-acf4-122deec2db2f 33 fields · synced Jun 8, 2026