Identity
- Trade Name
- Tealmed FDA UDI
- Generic Name
- Percussion hammer, manual, reusable FDA UDI
- Model / Reference
- #DH-3692 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06974546524365 FDA UDI
- FDA Product Code
- FZY FDA UDI
- GMDN Term
- Percussion hammer, manual, reusable 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
Yes
FDA UDI
Category: Percussion hammer, manual, reusable
Tealmed by Ningbo Tealmed Emergency Products Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Percussion hammer, manual, reusable.
- V. Mueller — STERIS CORPORATION · Class I
- BV Medical — Medical, Inc. · Class I
- Sklar® — Sklar Corporation · Class I
- Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
- Taylor Hammer — N S SURGICAL COMPANY · Class I
- BV Medical — Medical, Inc. · Class I
- hammer — Rashman Corp. · Class I
- Sklar® — Sklar Corporation · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ningbo Tealmed Emergency Products Co., Ltd.
Sources (1)
- FDA UDI 3868a715-9e38-40f0-85e9-b5b7b65b8609 32 fields · synced May 31, 2026