Identity
- Trade Name
- Jeato 7 Incontinence Clamp FDA UDI
- Generic Name
- Incontinence penis clamp, reusable FDA UDI
- Model / Reference
- JC002 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800064400103 FDA UDI
- FDA Product Code
- FHA FDA UDI
- GMDN Term
- Incontinence penis clamp, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.5160 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Incontinence penis clamp, reusable
Jeato 7 Incontinence Clamp by Jeato Med. CO., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Incontinence penis clamp, reusable.
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- Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class I
- Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · Class I
- KNUTSON URETHROGRAPHY CLAMP — SONTEC INSTRUMENTS, INC. · Class I
- Incontinence Clamp — C. R. Bard, Inc. · Class I
- Greenwald Surgical Company, Inc. — GRACE MANUFACTURING INC · 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 |
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Manufacturer
- Manufacturer
- Jeato Med. CO., Ltd.
Sources (1)
- FDA UDI 66c0ef46-9b0d-4bd8-a8fd-63bcde9f0852 32 fields · synced Jun 8, 2026