Identity
- Trade Name
- MT FDA UDI
- Generic Name
- Dermatome set, manual FDA UDI
- Model / Reference
- MT-3c FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06975808860726 FDA UDI
- FDA Product Code
- GES FDA UDI
- GMDN Term
- Dermatome set, manual FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dermatome set, manual
Mt by Jiangsu MJD Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- MT — Jiangsu MJD Medical Technology Co., Ltd. · Class I
- MT — Jiangsu MJD Medical Technology Co., Ltd. · 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
- Jiangsu MJD Medical Technology Co., Ltd.
Sources (1)
- FDA UDI f7d55c45-89c2-490f-b48c-29394260ceb2 32 fields · synced Jun 1, 2026