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H&H Emergency Cricothyrotomy Kit

FDA UDI

Class II (US FDA UDI)

by H & H Medical Corporation

Identity

Trade Name
H&H Emergency Cricothyrotomy Kit FDA UDI
Generic Name
Cricothyrotomy kit, single-use FDA UDI
Device Name
One time use sterile emergency airway kit that contains (1) Disposable Scalpel #10 blade, (1) Endotracheal Tube, 6.0 mm cuffed, (1) Curved Crile Hemostat, (1) News Tracheal Hook, (1) 10 cc syringe, (1) 35 cm Bougie and Twill Tape. FDA UDI
Model / Reference
Version 5 FDA UDI
Description
One time use sterile emergency airway kit that contains (1) Disposable Scalpel #10 blade, (1) Endotracheal Tube, 6.0 mm cuffed, (1) Curved Crile Hemostat, (1) News Tracheal Hook, (1) 10 cc syringe, (1) 35 cm Bougie and Twill Tape. FDA UDI

Identifiers

Catalog Number
HHECT01 FDA UDI
Primary DI / UDI-DI
00857048006002 FDA UDI
FDA Product Code
OGP FDA UDI
GMDN Term
Cricothyrotomy kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Height — 1.75 Inch FDA UDI
Width — 4.0 Inch FDA UDI
Length — 9.25 Inch FDA UDI

Category: Cricothyrotomy kit, single-use

H&H Emergency Cricothyrotomy Kit by H & H Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cricothyrotomy kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dc61bcec-62d4-427b-9388-0ca0e7aad755 36 fields · synced May 30, 2026