← Back to catalogue

Assi

FDA UDI

Class II (US FDA UDI)

by Accurate Surgical & Scientific Instruments Corp.

Identity

Trade Name
ASSI FDA UDI
Generic Name
Fibreoptic light cable FDA UDI
Device Name
Adapter for Fiber Optic Headlight Storz Type FDA UDI
Model / Reference
ASSI.FOAHL280 FDA UDI
Description
Adapter for Fiber Optic Headlight Storz Type FDA UDI

Identifiers

Primary DI / UDI-DI
00841645131861 FDA UDI
FDA Product Code
FCW FDA UDI
GMDN Term
Fibreoptic light cable 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fibreoptic light cable

Assi by Accurate Surgical & Scientific Instruments Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic light cable.

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
Accurate Surgical & Scientific Instruments Corp.

Sources (1)

  • FDA UDI 7b5f3aa0-6d67-46fa-9125-c1c6f971117c 33 fields · synced Jun 8, 2026