Identity
- Trade Name
- Curaplex FDA UDI
- Generic Name
- Emesis bag FDA UDI
- Device Name
- Curaplex Emesis Bag, 1000cc, Clear, Cardboard Rim w/o Hand Protection 25/pk 10pk/cs FDA UDI
- Model / Reference
- 1071-10208 FDA UDI
- Description
- Curaplex Emesis Bag, 1000cc, Clear, Cardboard Rim w/o Hand Protection 25/pk 10pk/cs FDA UDI
Identifiers
- Catalog Number
- 1071-10208 FDA UDI
- Primary DI / UDI-DI
- 00810071633577 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Emesis bag
Curaplex by Bound Tree Medical, 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
- ASP MEDICAL — Asp Global, LLC · Class I
- EmesEase Emesis Bag — Typenex Medical, LLC · Class I
- 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
- 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
- Bound Tree Medical, Llc
Sources (1)
- FDA UDI c6dcaf20-d53e-473a-a92d-e566f347c781 34 fields · synced Jun 8, 2026