IRIS Cervical hook

FDA UDI

Class I (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name: IRIS Cervical hook FDA UDI
Generic Name: Soft-tissue surgical hook, reusable FDA UDI
Device Name: IRIS Cervical hook FDA UDI
Model / Reference: 36-625 FDA UDI
Description: IRIS Cervical hook FDA UDI

Identifiers

Primary DI / UDI-DI: 00888937019698 FDA UDI
FDA Product Code: HFB FDA UDI
GMDN Term: Soft-tissue surgical hook, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.4530 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Soft-tissue surgical hook, reusable

IRIS Cervical hook by CooperSurgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: CooperSurgical, Inc.

Sources (1)

FDA UDI cee2546c-a5a4-4741-8cc6-1c6c34cbc065 33 fields · synced Jun 9, 2026