FDA UDI
In Commercial Distribution
🇺🇸 United States
Vertessa Lite 10x26cm
DI: 00890594000360
·
Model: CAL-VL1026
·
Caldera Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
Basic Information
- Brand Name
- Vertessa Lite 10x26cm
- Primary DI
- 00890594000360
- Version / Model
- CAL-VL1026
- Company Name
- Caldera Medical, Inc.
- Labeler DUNS
- 130341956
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-05-27
- Public Version
- 6
- Public Version Date
- 2022-07-19
- Public Version Status
- Update
- Public Device Record Key
- d6d14463-96bd-4704-8bfd-b7761259eb91
Device Description
Vertessa Lite 10x26cm polypropylene mesh for sacrocolpopexy
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- 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
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| OTO | Mesh, Surgical, Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed | General, Plastic Surgery | 878.3300 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 59676 | Pelvic organ prolapse surgical mesh, composite-polymer | A woven/knitted or porous material comprised of both a bioabsorbable polymer (e.g., poliglecaprone 25) and a non-bioabsorbable polymer (e.g., polypropylene) intended to be permanently implanted into a female patient for reinforcement and/or bridging of the supporting tissues of the pelvic floor for the surgical treatment of vaginal pelvic organ prolapse (POP), including anterior, posterior, or apical prolapse repair. It is typically available with various material attributes (e.g., density, pore size, weave) and may be pre-configured for specific repair or cut to desired size/shape. Disposable devices associated with implantation (e.g., introducer needles, trocars) may be included. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00890594000360 | GS1 | ||||
| Package | 00890594000353 | GS1 | box | 1 | In Commercial Distribution | |
| Package | 00890594000346 | GS1 | box | 3 | In Commercial Distribution |
Customer Contacts
- Phone
- 1-818-879-6555
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K150016 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | 10x26cm |
Storage Conditions
- Type
- Special Storage Condition, Specify
- Special Conditions
- This product must be stored at room temperature in a clean dry place. Do not expose product to direct sunlight, humid environments, or extreme temperatures. Do not use after expiration date.