Teleflex Minispacer

FDA UDI

Class II (US FDA UDI)

by Thayer Medical Corporation

Identity

Trade Name: TELEFLEX MINISPACER FDA UDI
Generic Name: Metered dose inhaler FDA UDI
Device Name: DUAL SPRAY MDI ADAPTER WITH 22MM O.D. X 22MM I.D. CONNECTIONS FDA UDI
Model / Reference: 1759 FDA UDI
Description: DUAL SPRAY MDI ADAPTER WITH 22MM O.D. X 22MM I.D. CONNECTIONS FDA UDI

Identifiers

Catalog Number: 1759 FDA UDI
Primary DI / UDI-DI: 00383480017592 FDA UDI
FDA Product Code: CAF FDA UDI
GMDN Term: Metered dose inhaler FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5630 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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Metered dose inhaler

Teleflex Minispacer by Thayer Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 II	Pending data

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Manufacturer

Manufacturer: Thayer Medical Corporation

Sources (1)

FDA UDI 745d5ec1-37de-4f54-802a-77d7db225961 35 fields · synced Jun 6, 2026