FDA UDI
In Commercial Distribution
🇺🇸 United States
CALICO
DI: 00850044458523
·
Model: FD007
·
Calico Medical Group LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10
Basic Information
- Brand Name
- CALICO
- Primary DI
- 00850044458523
- Version / Model
- FD007
- Catalog Number
- FD007
- Company Name
- Calico Medical Group LLC
- Labeler DUNS
- 118744421
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 10
- Record Status
- Published
- Publish Date
- 2022-08-19
- Public Version
- 1
- Public Version Date
- 2022-08-29
- Public Version Status
- New
- Public Device Record Key
- 087634a4-cc2b-4586-b6e8-6ba8f55520f7
Device Description
AG Silver Silicone Foam Dressing, Bordered, 2" x 2"
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
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- No
- Has Manufacturing Date
- No
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| FRO | Dressing, Wound, Drug | Unknown | U |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 47045 | Cavity-wound management dressing, antimicrobial | A non-bioabsorbable material or substance designed to be inserted into a wound bed to create an appropriate environment for healing (e.g., warm, moist, absorbent), and that contains an antimicrobial agent [e.g., silver (Ag), honey]. It is typically used for the management of deep secondary-healing wounds, particularly for indications such as stage III and IV pressure ulcers, deep leg ulcers, cavity wounds, excisions, and post-op wound dehiscence. It is often designed to conform to the wound bed to support tissues and is often nonadherent to provide for patient comfort during wound management. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 20850044458527 | GS1 | Case | 80 | In Commercial Distribution | |
| Primary | 00850044458523 | GS1 | ||||
| Unit of Use | 10850044458520 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K191819 | 000 |