← Back to catalogue

Custom Cut Silicone Sheeting For Internal Nasal Splints & Packing

FDA UDI

Class I (US FDA UDI)

by Invotec International, Inc.

Identity

Trade Name
Custom Cut Silicone Sheeting For Internal Nasal Splints & Packing FDA UDI
Generic Name
Intranasal splint, non-biodegradable FDA UDI
Device Name
Custom Cut Silicone Sheeting For Internal Nasal Splints & Packing, 2.2 X 3.0 X 0.020" Singles FDA UDI
Model / Reference
20-10682S FDA UDI
Description
Custom Cut Silicone Sheeting For Internal Nasal Splints & Packing, 2.2 X 3.0 X 0.020" Singles FDA UDI

Identifiers

Catalog Number
20-10682S FDA UDI
Primary DI / UDI-DI
00818501021062 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intranasal splint, non-biodegradable

Custom Cut Silicone Sheeting For Internal Nasal Splints & Packing by Invotec International, Inc. — Class I — FDA UDI — listed in FDA GUDID

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 7c96dc4f-d130-4517-b623-a6100c3b1d76 34 fields · synced Jun 9, 2026