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Symmetry Glassman

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Glassman FDA UDI
Generic Name
Clamp manipulation forceps FDA UDI
Device Name
Symmetry® Clamp, Glassman Instrument, Non-Crushing, 1 in Jaw, 250 mm FDA UDI
Model / Reference
37-4004 FDA UDI
Description
Symmetry® Clamp, Glassman Instrument, Non-Crushing, 1 in Jaw, 250 mm FDA UDI

Identifiers

Catalog Number
37-4004 FDA UDI
Primary DI / UDI-DI
00887482011836 FDA UDI
FDA Product Code
FFN FDA UDI
GMDN Term
Clamp manipulation forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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 — 250 Millimeter FDA UDI

Category: Clamp manipulation forceps

Symmetry Glassman by Symmetry Surgical Inc. — Class I — 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 c5833e1b-9e8b-4cba-86e2-58bbe97f46fb 36 fields · synced May 30, 2026