FDA UDI
In Commercial Distribution
🇺🇸 United States
Integra® Miltex® HeliTape®
DI: 10381780000303
·
Model: 62202
·
Integra Lifesciences Corporation
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
10
Basic Information
- Brand Name
- Integra® Miltex® HeliTape®
- Primary DI
- 10381780000303
- Version / Model
- 62202
- Catalog Number
- 62-202
- Company Name
- Integra Lifesciences Corporation
- Labeler DUNS
- 083171244
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 10
- Record Status
- Published
- Publish Date
- 2014-09-11
- Public Version
- 10
- Public Version Date
- 2023-05-04
- Public Version Status
- Update
- Public Device Record Key
- 6eb777a5-494f-417c-acec-43abe7fe5d46
Device Description
HeliPlug ® ABSORBABLE COLLAGEN Wound Dressing, 3/8in x 3/4in
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
- No
- 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 |
|---|---|---|---|---|
| LPG | Material, Dressing, Surgical, Polylactic Acid | Unknown | 3 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 47184 | General oral wound dressing, animal-derived | A collagen protein matrix derived from animal products (e.g., porcine, bovine) intended to be used as a protective cover for the general oral mucosa to manage wounds and sores in the mouth such as ulcers (non-infected or viral), periodontal surgical wounds, suture sites, burns, extraction sites, surgical wounds, and traumatic wounds; it may in addition, or alternatively, be intended to treat mucosal irritations/inflammation, dryness, and/or gingivitis. It may be supplied in various forms (e.g., gel, paste, fluid, water/oil spray solution) for use in the home or a clinical setting. After application, this device cannot be reused. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 30381780000307 | GS1 | CASE | 4 | In Commercial Distribution | |
| Primary | 10381780000303 | GS1 | ||||
| Secondary | H834622021 | HIBCC | ||||
| Unit of Use | 00381780000306 | GS1 |
Customer Contacts
- Phone
- +1(800)654-2873
- [email protected]
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | 1 cm x 2 cm | ||
| Device Size Text, specify | 3/8 in x 3/4 in |
Storage Conditions
- Type
- Special Storage Condition, Specify
- Special Conditions
- Avoid excessive heat and humidity