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Symmetry Crawford

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Crawford FDA UDI
Generic Name
Ophthalmic soft-tissue surgical forceps probe-tip, reusable FDA UDI
Device Name
Symmetry® Set, Crawford Lacrimal Intubation FDA UDI
Model / Reference
60-2014 FDA UDI
Description
Symmetry® Set, Crawford Lacrimal Intubation FDA UDI

Identifiers

Catalog Number
60-2014 FDA UDI
Primary DI / UDI-DI
00887482041116 FDA UDI
FDA Product Code
HNL FDA UDI
GMDN Term
Ophthalmic soft-tissue surgical forceps probe-tip, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Category: Ophthalmic soft-tissue surgical forceps probe-tip, reusable

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

Similar devices

Also classified as Ophthalmic soft-tissue surgical forceps probe-tip, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Symmetry Surgical Inc.

Sources (1)

  • FDA UDI eb9b8b6c-5d31-495c-9cd8-3c193939295d 35 fields · synced May 31, 2026