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Mini-Line

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
MINI-LINE FDA UDI
Generic Name
Surgical mist irrigation tip FDA UDI
Device Name
MINI-LINE SPRAY NOZZLE FDA UDI
Model / Reference
GB378 FDA UDI
Description
MINI-LINE SPRAY NOZZLE FDA UDI

Identifiers

Catalog Number
GB378 FDA UDI
Primary DI / UDI-DI
04038653288793 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Surgical mist irrigation tip FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical mist irrigation tip

Mini-Line by Aesculap, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical mist irrigation tip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 03e47245-93bf-4e77-aae4-3b3fbebda5f9 35 fields · synced Jun 8, 2026