Identity
- Trade Name
- RG Emergency Cric Kit FDA UDI
- Generic Name
- Cricothyrotomy kit, single-use FDA UDI
- Model / Reference
- RG-EMCRIC-001 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850029385028 FDA UDI
- GMDN Term
- Cricothyrotomy kit, single-use FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cricothyrotomy kit, single-use
RG Emergency Cric Kit by Regulus Global LLC — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Cricothyrotomy kit, single-use.
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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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Regulus Global LLC
Sources (1)
- FDA UDI 339ef27a-ce29-47b6-aa3d-8e45b25d2f5a 32 fields · synced Jun 8, 2026