Identity
- Trade Name
- Pinnakle Moderate Underpad FDA UDI
- Generic Name
- Absorbent underpad, non-antimicrobial, single-use FDA UDI
- Device Name
- Pinnakle Moderate Underpads are intended for use in protecting patients and elderly individuals experiencing urinary incontinence, individuals undergoing post-operative, postpartum women, and newborns FDA UDI
- Model / Reference
- 50 FDA UDI
- Description
- Pinnakle Moderate Underpads are intended for use in protecting patients and elderly individuals experiencing urinary incontinence, individuals undergoing post-operative, postpartum women, and newborns FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08938504806793 FDA UDI
- FDA Product Code
- KME FDA UDI
- GMDN Term
- Absorbent underpad, non-antimicrobial, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6060 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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Absorbent underpad, non-antimicrobial, single-use
Pinnakle Moderate Underpad by Phu Bao Group Company Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Absorbent underpad, non-antimicrobial, single-use.
- AmerisourceBergen — BP PHARMACEUTICALS LABORATORIES UNLIMITED COMPANY · Class I
- Sage TAP LC — SAGE PRODUCTS LLC · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- CUSTOMED — Customed, Inc. · Class I
- Abena — ABENA NORTH AMERICA, INC. · Class I
- Sures — VIVE HEALTH LLC · Class I
- Invenio — GRI Medical & Electronic Technology Co., Ltd. · Class I
- (Design) Cardinal Wings — Cardinal Health 200, LLC · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Phu Bao Group Company Limited
Sources (1)
- FDA UDI 7775cf0e-120a-40e5-bb07-f2359d146a42 33 fields · synced Jun 1, 2026