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Thermoplastic Nasal Splints

FDA UDI

Class I (US FDA UDI)

by Qfix

Identity

Trade Name
Thermoplastic Nasal Splints FDA UDI
Generic Name
External nasal splint FDA UDI
Device Name
Cosmetic Surgery Suppliers, Blush, 1/16", Trapezoidal Nasal Splint, pkg. of 10 FDA UDI
Model / Reference
THERM FDA UDI
Description
Cosmetic Surgery Suppliers, Blush, 1/16", Trapezoidal Nasal Splint, pkg. of 10 FDA UDI

Identifiers

Catalog Number
THERM FDA UDI
Primary DI / UDI-DI
10841962118702 FDA UDI
FDA Product Code
EPP FDA UDI
GMDN Term
External nasal splint FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.5800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Depth — .063 Inch FDA UDI

Category: External nasal splint

Thermoplastic Nasal Splints by Qfix — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External nasal splint.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Qfix

Sources (1)

  • FDA UDI 3df3f428-114c-4dc4-a795-6cf45ee8797f 36 fields · synced May 29, 2026