Identity
- Trade Name
- AART Pectoralis Implant Sizer FDA UDI
- Generic Name
- Pectoral implant FDA UDI
- Device Name
- Szr - Pectoral Sty 1 Sz 4 L NS FDA UDI
- Model / Reference
- B FDA UDI
- Description
- Szr - Pectoral Sty 1 Sz 4 L NS FDA UDI
Identifiers
- Catalog Number
- 500-104-5-2B FDA UDI
- Primary DI / UDI-DI
- B49050010452B0 FDA UDI
- 510(k) Number
- K021337 FDA UDI
- FDA Product Code
- MIC FDA UDI
- GMDN Term
- Pectoral implant FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.3620 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
AART Pectoralis Implant Sizer by Aart — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Aart
Sources (1)
- FDA UDI 4fb81e67-84d0-4742-8507-2bbd5bcc0fe7 37 fields · synced May 30, 2026