Repl Small Nasal Hood

FDA UDI

Class I (US FDA UDI)

by Parker Hannifin Corp.

Identity

Trade Name: REPL SMALL NASAL HOOD FDA UDI
Generic Name: Anaesthesia face mask, reusable FDA UDI
Device Name: REPL SMALL NASAL HOOD FDA UDI
Model / Reference: 91515094 FDA UDI
Description: REPL SMALL NASAL HOOD FDA UDI

Identifiers

Catalog Number: 91515094 FDA UDI
Primary DI / UDI-DI: 00816711021216 FDA UDI
FDA Product Code: KHA FDA UDI
GMDN Term: Anaesthesia face mask, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5590 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Anaesthesia face mask, reusable

Repl Small Nasal Hood by Parker Hannifin Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Anaesthesia face mask, reusable.

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AincA® — Anesthesia Associates, Inc. · Class I
Anesthesia Face Mask Pre-Filled Inflatable Single Use Large Adult Size 5 — FLEXICARE MEDICAL LIMITED · Class I
AincA® — Anesthesia Associates, Inc. · Class I
O-Two — O-Two Medical Technologies Inc · Class I
AincA® — Anesthesia Associates, Inc. · 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: Parker Hannifin Corp.

Sources (1)

FDA UDI 26515cdd-040d-4807-8ed6-720554078703 34 fields · synced May 29, 2026