← Back to catalogue

Crown Surgical

FDA UDI

Class I (US FDA UDI)

by Crown Surgical Corporation

Identity

Trade Name
CROWN SURGICAL FDA UDI
Generic Name
Suturing needle holder, single-use FDA UDI
Device Name
MAYO-HEGAR Needle Holder, 5-1/2" FDA UDI
Model / Reference
NEEDLE HOLDER FDA UDI
Description
MAYO-HEGAR Needle Holder, 5-1/2" FDA UDI

Identifiers

Catalog Number
16-286 FDA UDI
Primary DI / UDI-DI
B924162860 FDA UDI
FDA Product Code
FHQ FDA UDI
GMDN Term
Suturing needle holder, single-use 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Suturing needle holder, single-use

Crown Surgical by Crown Surgical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing needle holder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d396cefa-4133-4a99-acc1-dbfc2c58ec51 35 fields · synced May 30, 2026