Aed

FDA UDI

Class I (US FDA UDI)

by National Advanced Endoscopy Devices, Inc.

Identity

Trade Name: AED FDA UDI
Generic Name: Hand-held surgical retractor, reusable FDA UDI
Device Name: Laparoscopic Band Retractor with Nylon Handle, 5mm X 33cm FDA UDI
Model / Reference: LB1670-5 FDA UDI
Description: Laparoscopic Band Retractor with Nylon Handle, 5mm X 33cm FDA UDI

Identifiers

Primary DI / UDI-DI: 00848657066556 FDA UDI
FDA Product Code: NWV FDA UDI
GMDN Term: Hand-held surgical retractor, 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: Hand-held surgical retractor, reusable

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

Similar devices

Also classified as Hand-held surgical retractor, reusable.

ATLAS — ATLAS CERRAHİ ALETLER LTD. ŞTİ. · Class I
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
MİKRO — SAMSUN MİKRO CERRAHİ ALETLER İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ · Class I
Gimmi — Gimmi GmbH · Class I
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
Sklar® — Sklar Corporation · Class I
BIOCOMPOSITE PLUS ANCHOR Ø3, 5 MM W/NEEDLE — BMT BAPS BİYO MALZEME SANAYİ VE TİCARET ANONİM ŞİRKETİ · Class III
Spreizer / Spreader — REDA Instrumente GmbH · 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: National Advanced Endoscopy Devices, Inc.

Sources (1)

FDA UDI 81c375f9-c04f-4ba7-90ea-30f3c78d657d 33 fields · synced May 31, 2026