Identity
- Trade Name
- Carnegie Surgical LLC FDA UDI
- Generic Name
- Airway tube forceps, single-use FDA UDI
- Device Name
- MAGILL Intubation forceps, Intubation aid, made of stainless steel, single use, size child, box of 10 pcs, length 8”/20 cm FDA UDI
- Model / Reference
- 304-082 FDA UDI
- Description
- MAGILL Intubation forceps, Intubation aid, made of stainless steel, single use, size child, box of 10 pcs, length 8”/20 cm FDA UDI
Identifiers
- Catalog Number
- 304-082 FDA UDI
- Primary DI / UDI-DI
- G1413040820 FDA UDI
- FDA Product Code
- HTD FDA UDI
- GMDN Term
- Airway tube forceps, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Airway tube forceps, single-use
Carnegie Surgical LLC by Carnegie Surgical LLC — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Carnegie Surgical LLC
Sources (1)
- FDA UDI 87d56dbe-fe28-411e-a2e8-c66b27feceb2 35 fields · synced Jun 6, 2026