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ProArmor

FDA UDI

Class II (US FDA UDI)

by US Endoscopy

Identity

Trade Name
ProArmor FDA UDI
Generic Name
Surgical instrument guard, single-use, sterile FDA UDI
Device Name
ProArmor endoscope tip protector, non-sterile protects the distal tip of an endoscope and other surgical equipment. FDA UDI
Model / Reference
00711624 FDA UDI
Description
ProArmor endoscope tip protector, non-sterile protects the distal tip of an endoscope and other surgical equipment. FDA UDI

Identifiers

Catalog Number
00711624 FDA UDI
Primary DI / UDI-DI
00724995190644 FDA UDI
FDA Product Code
OCU FDA UDI
GMDN Term
Surgical instrument guard, single-use, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical instrument guard, single-use, sterile

ProArmor by US Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument guard, single-use, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
US Endoscopy

Sources (1)

  • FDA UDI 5b08343e-6a21-4278-b32f-699f7fd27a02 36 fields · synced May 30, 2026