Identity
- Trade Name
- DALTON ASPIRATOR FDA UDI
- Generic Name
- Cricothyrotome, reusable FDA UDI
- Device Name
- ASPIRATOR, SUCTION DEVICE WITHOUT CANISTER. FDA UDI
- Model / Reference
- ASP FDA UDI
- Description
- ASPIRATOR, SUCTION DEVICE WITHOUT CANISTER. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815027011850 FDA UDI
- FDA Product Code
- JCX FDA UDI
- GMDN Term
- Cricothyrotome, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4780 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cricothyrotome, reusable
Dalton Aspirator by Dalton Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cricothyrotome, reusable.
- RUSCH — TELEFLEX INCORPORATED · Class II
- RUSCH — TELEFLEX INCORPORATED · Class II
- RUSCH — TELEFLEX INCORPORATED · Class II
- RUSCH — TELEFLEX INCORPORATED · Class II
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
- Dalton Medical Corp.
Sources (1)
- FDA UDI 867dcb32-f471-44ea-a915-bc83471de071 33 fields · synced May 30, 2026