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Aligned Medical Solutions

FDA UDI

Class II (US FDA UDI)

by Aligned Medical Solutions

Identity

Trade Name
Aligned Medical Solutions FDA UDI
Generic Name
Peripheral anaesthesia single-administration set, non-medicated FDA UDI
Device Name
NERVE BLOCK TRAY FDA UDI
Model / Reference
AMS7628A FDA UDI
Description
NERVE BLOCK TRAY FDA UDI

Identifiers

Catalog Number
AMS7628A FDA UDI
Primary DI / UDI-DI
B098AMS7628A0 FDA UDI
FDA Product Code
OGJ FDA UDI
GMDN Term
Peripheral anaesthesia single-administration set, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5140 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: Peripheral anaesthesia single-administration set, non-medicated

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

Similar devices

Also classified as Peripheral anaesthesia single-administration set, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cad00028-8093-4ea2-b700-8f2a0e05606a 36 fields · synced Jun 8, 2026