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Aed

FDA UDI

Class I (US FDA UDI)

by National Advanced Endoscopy Devices, Inc.

Identity

Trade Name
AED FDA UDI
Generic Name
Arthroscopic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Heavy Duty Arthroscopic Grasping Forceps FDA UDI
Model / Reference
17-1850 FDA UDI
Description
Heavy Duty Arthroscopic Grasping Forceps FDA UDI

Identifiers

Primary DI / UDI-DI
00848657014724 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Arthroscopic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Arthroscopic surgical procedure kit, non-medicated, reusable

A comprehensive medical device directory, featuring the AED Arthroscopic surgical procedure kit. This reusable device is used in orthopedic surgeries and is designed for specific use in arthroscopic procedures.

Similar devices

Also classified as Arthroscopic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
National Advanced Endoscopy Devices, Inc.

Sources (1)

  • FDA UDI 9bbd03ae-bb6a-494e-8bc4-35e293446055 33 fields · synced Jul 1, 2026