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Symmetry Verity™

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Verity™ FDA UDI
Generic Name
Wire/ligature passer, reusable FDA UDI
Device Name
Verity™ Passer, Ligature, Titanium Handle, 3.0 mm Hook, Stainless Steel Shaft, 7 3/4 in FDA UDI
Model / Reference
80-1530 FDA UDI
Description
Verity™ Passer, Ligature, Titanium Handle, 3.0 mm Hook, Stainless Steel Shaft, 7 3/4 in FDA UDI

Identifiers

Catalog Number
80-1530 FDA UDI
Primary DI / UDI-DI
00887482031063 FDA UDI
FDA Product Code
HCF FDA UDI
GMDN Term
Wire/ligature passer, reusable 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

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
Width — 3 Millimeter FDA UDI
Length — 7.75 Inch FDA UDI

Category: Wire/ligature passer, reusable

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

Similar devices

Also classified as Wire/ligature passer, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3e9a1221-2887-45eb-9616-89864fae98e2 36 fields · synced May 31, 2026