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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
Skin-coring punch, reusable FDA UDI
Device Name
Symmetry® Punch; Symmetry; 3 mm; 8 in FDA UDI
Model / Reference
51-1087 FDA UDI
Description
Symmetry® Punch; Symmetry; 3 mm; 8 in FDA UDI

Identifiers

Catalog Number
51-1087 FDA UDI
Primary DI / UDI-DI
00887482021460 FDA UDI
FDA Product Code
HAE FDA UDI
GMDN Term
Skin-coring punch, reusable 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

Dimensions & Sizes

Size
Length — 8 Inch FDA UDI
Width — 3 Millimeter FDA UDI

Category: Skin-coring punch, reusable

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

Similar devices

Also classified as Skin-coring punch, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eb8bf74b-7f9b-407a-a616-caf824d54930 36 fields · synced Jun 8, 2026