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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
ENT foreign body inflatable extractor FDA UDI
Device Name
Surex Sural Nerve Extractor 43cm for harvesting Sural Nerve Grafts FDA UDI
Model / Reference
ASSI.AG78826 FDA UDI
Description
Surex Sural Nerve Extractor 43cm for harvesting Sural Nerve Grafts FDA UDI

Identifiers

Primary DI / UDI-DI
00841645129462 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
ENT foreign body inflatable extractor 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: ENT foreign body inflatable extractor

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

Similar devices

Also classified as ENT foreign body inflatable extractor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Accurate Surgical & Scientific Instruments Corp.

Sources (1)

  • FDA UDI cebf8a6c-ca22-43a7-9192-c3b726aed4a8 33 fields · synced Jun 6, 2026