Identity
- Trade Name
- Coag it NASAL PACK FDA UDI
- Generic Name
- Intranasal splint, non-biodegradable FDA UDI
- Device Name
- Coag it NASAL PACK (dual pouch, single unit) FDA UDI
- Model / Reference
- CC0009A FDA UDI
- Description
- Coag it NASAL PACK (dual pouch, single unit) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860003566534 FDA UDI
- FDA Product Code
- EMX FDA UDI
- GMDN Term
- Intranasal splint, non-biodegradable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4100 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
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
No
FDA UDI
Category: Intranasal splint, non-biodegradable
Coag it NASAL PACK by Coagco Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Custom Nasal Splint — Boston Medical Products, Inc. · Class I
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
- Coagco Llc
Sources (1)
- FDA UDI dd695974-cc62-4d66-bbd4-242a9eb97a9a 33 fields · synced Jun 8, 2026