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Symmetry Tischler

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Tischler FDA UDI
Generic Name
Skin-coring punch, reusable FDA UDI
Device Name
Symmetry® Punch, Tischler Biopsy, 3 x 7 mm Bite, 10 in FDA UDI
Model / Reference
52-6556 FDA UDI
Description
Symmetry® Punch, Tischler Biopsy, 3 x 7 mm Bite, 10 in FDA UDI

Identifiers

Catalog Number
52-6556 FDA UDI
Primary DI / UDI-DI
00887482078273 FDA UDI
FDA Product Code
LRY FDA UDI
GMDN Term
Skin-coring punch, 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
Depth — 7 Millimeter FDA UDI
Length — 10 Inch FDA UDI

Category: Skin-coring punch, reusable

Symmetry Tischler by Symmetry Surgical Inc. — Class I — 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 0bfa75e0-2747-4bc2-af10-a383cda94df9 36 fields · synced Jun 8, 2026