Doyle Combo Splint

FDA UDI

Class I (US FDA UDI)

by Boston Medical Products, Inc.

Identity

Trade Name: Doyle Combo Splint FDA UDI
Generic Name: Intranasal splint, non-biodegradable FDA UDI
Model / Reference: 60-202 FDA UDI

Identifiers

Catalog Number: 60-202 FDA UDI
Primary DI / UDI-DI: EBES602020 FDA UDI
510(k) Number: K972151 FDA UDI
FDA Product Code: LYA FDA UDI
GMDN Term: Intranasal splint, non-biodegradable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4780 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

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

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Intranasal splint, non-biodegradable

Doyle Combo Splint by Boston Medical Products, Inc. — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Boston Medical Products, Inc.

Sources (1)

FDA UDI 8dd568b2-b221-4f5d-8eda-b0bc1ffa10ef 36 fields · synced Jun 9, 2026