Identity
- Trade Name
- ReadyCric 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) 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) 10 cc syringe, (1) 35 cm Bougie and Twill Tape. FDA UDI
Identifiers
- Catalog Number
- HHRCK01 FDA UDI
- Primary DI / UDI-DI
- 00857048006477 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
- Length — 9.25 Inch FDA UDIWidth — 4.0 Inch FDA UDIHeight — 1.75 Inch FDA UDI
Category: Cricothyrotomy kit, single-use
ReadyCric Kit by H & H Medical Corporation — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- H & H Medical Corporation
Sources (1)
- FDA UDI 6e08c28b-a2f5-46ee-9612-8660a0f6ac03 36 fields · synced Jun 8, 2026