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Nathan

FDA UDI

Class I (US FDA UDI)

by Doctor Shock Inc

Identity

Trade Name
Nathan FDA UDI
Generic Name
Orthotic insole, prefabricated, non-antimicrobial FDA UDI
Device Name
Sunglasses FDA UDI
Model / Reference
NS10340-00001-OSFM FDA UDI
Description
Sunglasses FDA UDI

Identifiers

Primary DI / UDI-DI
00717064949335 FDA UDI
FDA Product Code
HQY FDA UDI
GMDN Term
Orthotic insole, prefabricated, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.5850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Category: Orthotic insole, prefabricated, non-antimicrobial

Nathan by Doctor Shock Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthotic insole, prefabricated, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Doctor Shock Inc

Sources (1)

  • FDA UDI 99d18cf2-64af-4b06-ad01-aa7e4b8b24a2 33 fields · synced Jun 8, 2026