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Assi

FDA UDI

Class I (US FDA UDI)

by Accurate Surgical & Scientific Instruments Corp.

Identity

Trade Name
ASSI FDA UDI
Generic Name
Fibreoptic retractor handle FDA UDI
Device Name
Epstein Breast Retractor 90x27mm blade, w/Fiber Optic & Reversed Suction tube, 36mm spatulated working end with teeth FDA UDI
Model / Reference
ASSI.ABR30626 FDA UDI
Description
Epstein Breast Retractor 90x27mm blade, w/Fiber Optic & Reversed Suction tube, 36mm spatulated working end with teeth FDA UDI

Identifiers

Primary DI / UDI-DI
00841645142362 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Fibreoptic retractor handle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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 retractor handle

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

Similar devices

Also classified as Fibreoptic retractor handle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 74ce689c-3ce1-4ad6-b50b-707eac3c4c52 33 fields · synced Jun 6, 2026