Identity
- Trade Name
- XS FDA UDI
- Generic Name
- General-purpose surgical scissors, reusable FDA UDI
- Device Name
- PERNECZKY/CRISTANTE XS Micro scissors, jaw inserts, straight, 2 3/4", (70 mm), blunt/blunt, with tubular shaft, non-sterile, reusable FDA UDI
- Model / Reference
- FM695R FDA UDI
- Description
- PERNECZKY/CRISTANTE XS Micro scissors, jaw inserts, straight, 2 3/4", (70 mm), blunt/blunt, with tubular shaft, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- FM695R FDA UDI
- Primary DI / UDI-DI
- 04038653263257 FDA UDI
- FDA Product Code
- GZX FDA UDI
- GMDN Term
- General-purpose surgical scissors, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4525 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Xs by Aesculap, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Aesculap, Inc.
Sources (1)
- FDA UDI df31b7c2-4d12-43c5-beff-39c3e3c0bb21 37 fields · synced Jun 8, 2026