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Removal System, Screw, Legacy, Broken & Stripped Extractors MKS1022
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Removal System, Screw, Legacy, Broken & Stripped Extractors MKS1022 FDA UDI
- Generic Name
- Screw extractor, single-use FDA UDI
- Device Name
- STRIPPED SCREW TIP M7 FDA UDI
- Model / Reference
- TP352-M01 FDA UDI
- Description
- STRIPPED SCREW TIP M7 FDA UDI
Identifiers
- Primary DI / UDI-DI
- B756TP352M01 FDA UDI
- FDA Product Code
- HWB FDA UDI
- GMDN Term
- Screw extractor, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Screw extractor, single-use
Removal System, Screw, Legacy, Broken & Stripped Extractors MKS1022 by Shukla Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Shukla Medical
Sources (1)
- FDA UDI e0befb13-5eaa-4e17-b54a-bb92c968830a 34 fields · synced Jun 1, 2026