Aed

FDA UDI

Class I (US FDA UDI)

by National Advanced Endoscopy Devices, Inc.

Identity

Trade Name: AED FDA UDI
Generic Name: Rigid endoscopic grasping forceps, reusable FDA UDI
Device Name: Chole Clamp with Ratchet Handle, 5mm X 33cm FDA UDI
Model / Reference: CL1249 FDA UDI
Description: Chole Clamp with Ratchet Handle, 5mm X 33cm FDA UDI

Identifiers

Primary DI / UDI-DI: 00848657066235 FDA UDI
FDA Product Code: NWV FDA UDI
GMDN Term: Rigid endoscopic grasping forceps, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.1720 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Rigid endoscopic grasping forceps, reusable

Aed by National Advanced Endoscopy Devices, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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ACUFEX / PITBULL — Smith & Nephew, Inc. · Class I
Endo — Smith & Nephew, Inc. · Class I
ACUFEX — Smith & Nephew, Inc. · Class I
gSource — GSOURCE, LLC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: National Advanced Endoscopy Devices, Inc.

Sources (1)

FDA UDI badebfa4-d1b7-4fd2-a931-355ead9ad358 33 fields · synced May 30, 2026