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H&H Simplified Cric Kit

FDA UDI

Class II (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
H&H Simplified Cric Kit FDA UDI
Generic Name
Cricothyrotome, single-use FDA UDI
Device Name
Simplified Cricothyrotomy Kit, 10/Case FDA UDI
Model / Reference
02 FDA UDI
Description
Simplified Cricothyrotomy Kit, 10/Case FDA UDI

Identifiers

Catalog Number
HHSCK01 FDA UDI
Primary DI / UDI-DI
M689HHSCK01020 FDA UDI
FDA Product Code
OGP FDA UDI
GMDN Term
Cricothyrotome, 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cricothyrotome, single-use

H&H Simplified Cric Kit by Safeguard Us Operating, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cricothyrotome, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 24021f99-cff9-4fa0-aeb0-a7c38823674a 35 fields · synced May 30, 2026