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Symmetry COOLEY

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry COOLEY FDA UDI
Generic Name
Clamp manipulation forceps FDA UDI
Device Name
Symmetry® Clamp; Cooley Anastomosis; 165 mm FDA UDI
Model / Reference
37-1210 FDA UDI
Description
Symmetry® Clamp; Cooley Anastomosis; 165 mm FDA UDI

Identifiers

Catalog Number
37-1210 FDA UDI
Primary DI / UDI-DI
00887482011324 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Clamp manipulation forceps FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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 — 165 Millimeter FDA UDI

Category: Clamp manipulation forceps

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

Similar devices

Also classified as Clamp manipulation forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 82d602b1-143c-4853-ad7c-22f4ebdcb53d 36 fields · synced May 30, 2026