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Avalign

FDA UDI

Class II (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name
Avalign FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
Prestige Type Retraction Grasper, rotatable, with ratchet FDA UDI
Model / Reference
VM46645345 FDA UDI
Description
Prestige Type Retraction Grasper, rotatable, with ratchet FDA UDI

Identifiers

Primary DI / UDI-DI
00190776004538 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Width — 5 Millimeter FDA UDI
Length — 45 Centimeter FDA UDI

Category: Rigid endoscopic tissue manipulation forceps, reusable

A versatile, rotatable, and ratchet-type retraction grasper designed for general surgical procedures. Its rigid design allows for precise tissue manipulation during endoscopic surgery.

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AVALIGN TECHNOLOGIES, Inc.

Sources (1)

  • FDA UDI cd95d34f-81f5-4751-b40a-a5f8574398ae 35 fields · synced Jul 10, 2026