Identity
- Trade Name
- ASP MEDICAL FDA UDI
- Generic Name
- Emesis bag FDA UDI
- Device Name
- EMESIS BAG, STANDARD 1000CC, 1/EA, 25/BG, 150/CS (6PK/CS) FDA UDI
- Model / Reference
- EGT205 FDA UDI
- Description
- EMESIS BAG, STANDARD 1000CC, 1/EA, 25/BG, 150/CS (6PK/CS) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840216102408 FDA UDI
- FDA Product Code
- FNY FDA UDI
- GMDN Term
- Emesis bag FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6730 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
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Emesis bag
Asp Medical by Asp Global, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Emesis bag.
- ProCure — Twin Med, LLC · Class I
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- NS30830 Emesis Bag Clear 40 oz. (1000ml) — XODUS MEDICAL, INC. · Class I
- Centurion — Centurion Medical Products · Class I
- Convenience Bag — Typenex Medical, LLC · Class I
- ProCure — Twin Med, LLC · Class I
- Curaplex — BOUND TREE MEDICAL, LLC · Class I
- Emesis Bag — Dynarex Corp. · 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
- Asp Global, LLC
Sources (1)
- FDA UDI 41c0f0f8-ef76-4e1a-9e0d-404c8bf6fdae 33 fields · synced Jun 8, 2026