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Avalign

FDA UDI

Class II (US FDA UDI)

by Progressive Medical Instrumentation Inc

Identity

Trade Name
AVALIGN FDA UDI
Generic Name
Orthopaedic joint/limb rongeur FDA UDI
Device Name
IVD RONG UP 5X10MM 11.75" FDA UDI
Model / Reference
PMI-LK75-2974/45 FDA UDI
Description
IVD RONG UP 5X10MM 11.75" FDA UDI

Identifiers

Catalog Number
PMI-LK75-2974/45 FDA UDI
Primary DI / UDI-DI
00850011214176 FDA UDI
FDA Product Code
HAE FDA UDI
GMDN Term
Orthopaedic joint/limb rongeur FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4840 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic joint/limb rongeur

Avalign by Progressive Medical Instrumentation Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic joint/limb rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 68cfeb8f-2bfd-42a5-a7ed-4c1e6c75d936 35 fields · synced Jun 1, 2026