FDA UDI
In Commercial Distribution
🇺🇸 United States
Monoart
DI: E307220300060
·
Model: Monoart Bib Up!
·
EURONDA SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Monoart
- Primary DI
- E307220300060
- Version / Model
- Monoart Bib Up!
- Catalog Number
- 22030006
- Company Name
- EURONDA SPA
- Labeler DUNS
- 428755441
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2025-04-10
- Public Version
- 1
- Public Version Date
- 2025-04-18
- Public Version Status
- New
- Public Device Record Key
- ee6b8bf2-503c-466c-a69a-6e2b6620cd67
Device Description
Disposable patient protection aprons consisting of a highly absorbent multiple-ply paper embossed with a waterproof polyethylene layer, without the use of glues. Soft and comfortable, compared to traditional towels, they offer larger dimensions and functional contouring on the neck and shoulders for complete patient protection and practical adhesives for fixing. Pack of 150 aprons. Colour: lime.
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- Yes
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| KHR | Absorber, Saliva, Paper | Dental | 872.6050 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 61048 | Patient examination/treatment drape, single-use | A non-sterile, noninvasive flat sheet designed to cover a portion of a patient’s anatomy during an examination or non-surgical treatment procedure in the home or healthcare facility primarily to prevent soiling/cross-contamination; it is not intended for surgical use. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | E307220300060 | HIBCC |