← Back to catalogue

Haritex Corporation

FDA UDI

Class I (US FDA UDI)

by Haritex Corporation

Identity

Trade Name
Haritex Corporation FDA UDI
Generic Name
Medical tubing clip/clamp, temporary, non-calibrated, single-use FDA UDI
Device Name
FORCEPS WIRE HEMO KELLY STR 5-1/2", SINGLE USE. FDA UDI
Model / Reference
HC-57 FDA UDI
Description
FORCEPS WIRE HEMO KELLY STR 5-1/2", SINGLE USE. FDA UDI

Identifiers

Catalog Number
HC-57 FDA UDI
Primary DI / UDI-DI
04719880180516 FDA UDI
FDA Product Code
HRQ FDA UDI
GMDN Term
Medical tubing clip/clamp, temporary, non-calibrated, 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical tubing clip/clamp, temporary, non-calibrated, single-use

Haritex Corporation by Haritex Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical tubing clip/clamp, temporary, non-calibrated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Haritex Corporation

Sources (1)

  • FDA UDI 24197e6f-b8f1-4fe7-8268-f91db5c1d0bf 34 fields · synced May 31, 2026