← Back to catalogue

Custom Nasal Splint

FDA UDI

Class I (US FDA UDI)

by Boston Medical Products, Inc.

Identity

Trade Name
Custom Nasal Splint FDA UDI
Generic Name
Intranasal splint, non-biodegradable FDA UDI
Device Name
Size: 0.25 x 51 x 76 mm; Type: FEP FDA UDI
Model / Reference
60-310 FDA UDI
Description
Size: 0.25 x 51 x 76 mm; Type: FEP FDA UDI

Identifiers

Catalog Number
60-310 FDA UDI
Primary DI / UDI-DI
EBES603100 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Height — 76 Millimeter FDA UDI
Length — 51 Millimeter FDA UDI
Width — 0.25 Millimeter FDA UDI

Category: Intranasal splint, non-biodegradable

Custom Nasal Splint by Boston Medical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intranasal splint, non-biodegradable.

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

Sources (1)

  • FDA UDI a5702922-4cae-4ccd-b61a-3dc7cd153e56 37 fields · synced Jun 9, 2026