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Symmetry Surgical

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Surgical FDA UDI
Generic Name
Haemorrhoid ligator FDA UDI
Device Name
Symmetry® Kit/Set, Hemorrhoidal Ligator, 8 in FDA UDI
Model / Reference
DX-8 FDA UDI
Description
Symmetry® Kit/Set, Hemorrhoidal Ligator, 8 in FDA UDI

Identifiers

Catalog Number
DX-8 FDA UDI
Primary DI / UDI-DI
00887482192870 FDA UDI
FDA Product Code
FHN FDA UDI
GMDN Term
Haemorrhoid ligator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4400 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

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

Dimensions & Sizes

Size
Length — 8 Inch FDA UDI

Category: Haemorrhoid ligator

Symmetry Surgical by Symmetry Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemorrhoid ligator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5562fc2a-2761-47e7-af6a-b2dd795b910d 36 fields · synced May 30, 2026