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Freeman Hook Retractor

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
FREEMAN HOOK RETRACTOR FDA UDI
Generic Name
Hand-held surgical retractor, reusable FDA UDI
Device Name
FREEMAN HOOK RETRACTOR SEVEN SHARP PRONGS WITH SHORTER INNER PRONGS FDA UDI
Model / Reference
475-505 FDA UDI
Description
FREEMAN HOOK RETRACTOR SEVEN SHARP PRONGS WITH SHORTER INNER PRONGS FDA UDI

Identifiers

Catalog Number
475-505 FDA UDI
Primary DI / UDI-DI
00192896042322 FDA UDI
FDA Product Code
KAL FDA UDI
GMDN Term
Hand-held surgical retractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI

Category: Hand-held surgical retractor, reusable

Freeman Hook Retractor by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 75e808be-4533-4eb3-8d07-ade9bbeb894f 36 fields · synced May 31, 2026