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Needle Holder

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
NEEDLE HOLDER FDA UDI
Generic Name
Suturing needle holder, single-use FDA UDI
Device Name
MAYO HEGAR N/H 6" SERRATED PAS FDA UDI
Model / Reference
MAYO HEGAR NEEDLE HOLDERS FDA UDI
Description
MAYO HEGAR N/H 6" SERRATED PAS FDA UDI

Identifiers

Catalog Number
MHN6PAS FDA UDI
Primary DI / UDI-DI
B974MHN6PAS0 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Suturing needle holder, single-use 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 6 Inch FDA UDI

Category: Suturing needle holder, single-use

Needle Holder by Dr.frigz International(pvt)ltd, — 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

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Manufacturer

Sources (1)

  • FDA UDI 92cd28df-f11b-4896-bbf0-9a02694e767e 35 fields · synced May 30, 2026