Identity
- Trade Name
- PRINCETON FDA UDI
- Generic Name
- Circumcision stapler/staple FDA UDI
- Device Name
- CIRCUMCISION INSTRUMENT 13MMØ FDA UDI
- Model / Reference
- 67240-13 FDA UDI
- Description
- CIRCUMCISION INSTRUMENT 13MMØ FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810158215726 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Circumcision stapler/staple 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Circumcision stapler/staple
Princeton by Princeton Medical Group, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Circumcision stapler/staple.
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- MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
- MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
- PRINCETON — PRINCETON MEDICAL GROUP, 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
- Princeton Medical Group, Inc.
Sources (1)
- FDA UDI 84de582d-f460-4185-85e9-1a4206f5b68b 33 fields · synced Jun 8, 2026