← Back to catalogue

Elan 4

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
ELAN 4 FDA UDI
Generic Name
Pneumatic surgical power tool hose FDA UDI
Device Name
ELAN 4 AIR MOTOR HOSE 5M W/HAND CONTROL FDA UDI
Model / Reference
GA707R FDA UDI
Description
ELAN 4 AIR MOTOR HOSE 5M W/HAND CONTROL FDA UDI

Identifiers

Catalog Number
GA707R FDA UDI
Primary DI / UDI-DI
04046963835309 FDA UDI
FDA Product Code
HBB FDA UDI
GMDN Term
Pneumatic surgical power tool hose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4370 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

No

FDA UDI

Lot / Batch Number

No

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: Pneumatic surgical power tool hose

Elan 4 by Aesculap, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pneumatic surgical power tool hose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI e836d4d8-36ac-45d1-abd5-72e41b610e2a 35 fields · synced Jun 1, 2026