← Back to catalogue

Aligned Medical Solutions

FDA UDI

Class I (US FDA UDI)

by Aligned Medical Solutions

Identity

Trade Name
Aligned Medical Solutions FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Toe Nail Clipper 5.5" FDA UDI
Model / Reference
AMS1079 FDA UDI
Description
Toe Nail Clipper 5.5" FDA UDI

Identifiers

Catalog Number
AMS1079 FDA UDI
Primary DI / UDI-DI
B098AMS10790 FDA UDI
FDA Product Code
LRP FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

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

Yes

FDA UDI

Category: General surgical procedure kit, non-medicated, single-use

Aligned Medical Solutions by Aligned Medical Solutions — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgical procedure kit, non-medicated, single-use.

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

Manufacturer
Aligned Medical Solutions

Sources (1)

  • FDA UDI 12a439c0-ddac-4e56-8945-57effd81cb2a 36 fields · synced Jun 8, 2026