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Retractor

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
RETRACTOR FDA UDI
Generic Name
Hand-held surgical retractor, single-use FDA UDI
Device Name
GOELET RETRACTOR 7 1/2" FDA UDI
Model / Reference
GOELET RETRACTOR FDA UDI
Description
GOELET RETRACTOR 7 1/2" FDA UDI

Identifiers

Catalog Number
504113 FDA UDI
Primary DI / UDI-DI
B97450411300 FDA UDI
FDA Product Code
EIG FDA UDI
GMDN Term
Hand-held surgical retractor, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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 — 7.5 Inch FDA UDI

Category: Hand-held surgical retractor, single-use

Retractor by Dr.frigz International(pvt)ltd, — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held surgical retractor, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dr.frigz International(pvt)ltd,

Sources (1)

  • FDA UDI d41cce37-c79c-4cc2-a206-723750849b34 35 fields · synced May 30, 2026