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Jedmed

FDA UDI

Class I (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name
JEDMED FDA UDI
Generic Name
Soft-tissue surgical hook, reusable FDA UDI
Device Name
HOOK RETRACTOR DOUBLE MILLARD FDA UDI
Model / Reference
52-4742 FDA UDI
Description
HOOK RETRACTOR DOUBLE MILLARD FDA UDI

Identifiers

Catalog Number
52-4742 FDA UDI
Primary DI / UDI-DI
M6335247420 FDA UDI
FDA Product Code
GDG FDA UDI
GMDN Term
Soft-tissue surgical hook, reusable 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

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

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: Soft-tissue surgical hook, reusable

Jedmed by JEDMED Instrument Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft-tissue surgical hook, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ed73554d-aec3-437d-824f-b4949d389a74 34 fields · synced Jun 8, 2026